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Items: 1 to 100 of 580

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr12:52301253
GRCh38:
Chr12:51907469
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Benign
(Jan 15, 2019)
criteria provided, single submitterVCV000811884
2.
GRCh37:
Chr12:52301283
GRCh38:
Chr12:51907499
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Likely benign
(Jan 13, 2018)
criteria provided, single submitterVCV000309435
3.
GRCh37:
Chr12:52301291
GRCh38:
Chr12:51907507
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000309436
4.
GRCh37:
Chr12:52301317
GRCh38:
Chr12:51907533
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000881402
5.
GRCh37:
Chr12:52301356
GRCh38:
Chr12:51907572
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000309437
6.
GRCh37:
Chr12:52301427
GRCh38:
Chr12:51907643
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000309438
7.
GRCh37:
Chr12:52301433
GRCh38:
Chr12:51907649
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Conflicting interpretations of pathogenicity
(Apr 28, 2020)
criteria provided, conflicting interpretationsVCV000309439
8.
GRCh37:
Chr12:52301439
GRCh38:
Chr12:51907655
ACVRL1not specified, Telangiectasia, hereditary hemorrhagic, type 2Benign
(Aug 27, 2018)
criteria provided, multiple submitters, no conflictsVCV000212792
9.
GRCh37:
Chr12:52305786
GRCh38:
Chr12:51912002
ACVRL1not providedBenign
(Jun 26, 2018)
criteria provided, single submitterVCV001271094
10.
GRCh37:
Chr12:52305789
GRCh38:
Chr12:51912005
ACVRL1not providedBenign
(Jun 26, 2018)
criteria provided, single submitterVCV001174347
11.
GRCh37:
Chr12:52306027
GRCh38:
Chr12:51912243
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2, not providedBenign
(Jul 22, 2018)
criteria provided, multiple submitters, no conflictsVCV000810906
12.
GRCh37:
Chr12:52306195
GRCh38:
Chr12:51912411
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Jan 6, 2019)
criteria provided, single submitterVCV000811874
13.
GRCh37:
Chr12:52306221
GRCh38:
Chr12:51912437
ACVRL1not specified, Telangiectasia, hereditary hemorrhagic, type 2Benign
(Jul 4, 2020)
criteria provided, multiple submitters, no conflictsVCV000136292
14.
GRCh37:
Chr12:52306249-52314687
GRCh38:
Chr12:51912465-51920903
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Nov 8, 2018)
criteria provided, single submitterVCV000657392
15.
GRCh37:
Chr12:52306255
GRCh38:
Chr12:51912471
ACVRL1not providedUncertain significance
(Jun 1, 2017)
criteria provided, single submitterVCV000444295
16.
GRCh37:
Chr12:52306263
GRCh38:
Chr12:51912479
ACVRL1T2ITelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Jun 18, 2020)
criteria provided, single submitterVCV000850758
17.
GRCh37:
Chr12:52306267
GRCh38:
Chr12:51912483
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Conflicting interpretations of pathogenicity
(Sep 3, 2020)
criteria provided, conflicting interpretationsVCV000698538
18.
GRCh37:
Chr12:52306282
GRCh38:
Chr12:51912498
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Likely benign
(Aug 6, 2020)
criteria provided, single submitterVCV001161010
19.
GRCh37:
Chr12:52306295
GRCh38:
Chr12:51912511
ACVRL1L13fsPulmonary arterial hypertension related to hereditary hemorrhagic telangiectasiaPathogenicno assertion criteria providedVCV000426009
20.
GRCh37:
Chr12:52306298-52306299
GRCh38:
Chr12:51912514-51912515
ACVRL1M15fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jul 3, 2017)
criteria provided, single submitterVCV000411301
21.
GRCh37:
Chr12:52306316
GRCh38:
Chr12:51912532
ACVRL1Q20*Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Aug 23, 2019)
criteria provided, single submitterVCV000533342
22.
GRCh37:
Chr12:52306341
GRCh38:
Chr12:51912557
ACVRL1not specified, not providedBenign
(Aug 15, 2018)
criteria provided, multiple submitters, no conflictsVCV000439370
23.
GRCh37:
Chr12:52306687
GRCh38:
Chr12:51912903
ACVRL1not providedBenign
(Jun 26, 2018)
criteria provided, single submitterVCV001226999
24.
GRCh37:
Chr12:52306814
GRCh38:
Chr12:51913030
ACVRL1not provided, Telangiectasia, hereditary hemorrhagic, type 2Benign/Likely benign
(Aug 15, 2018)
criteria provided, multiple submitters, no conflictsVCV000811494
25.
GRCh37:
Chr12:52306863-52307574
GRCh38:
Chr12:51913079-51913790
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Dec 11, 2017)
criteria provided, single submitterVCV000533360
26.
GRCh37:
Chr12:52306890
GRCh38:
Chr12:51913106
ACVRL1not provided, Telangiectasia, hereditary hemorrhagic, type 2Likely benign
(Oct 1, 2018)
criteria provided, single submitterVCV000753239
27.
GRCh37:
Chr12:52306891-52306898
GRCh38:
Chr12:51913107-51913114
ACVRL1K25fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Dec 4, 2018)
criteria provided, single submitterVCV000811218
28.
GRCh37:
Chr12:52306898
GRCh38:
Chr12:51913114
ACVRL1P26LTelangiectasia, hereditary hemorrhagic, type 2Likely benign
(May 26, 2020)
criteria provided, single submitterVCV000698484
29.
GRCh37:
Chr12:52306899-52306902
GRCh38:
Chr12:51913115-51913118
ACVRL1S27fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jun 27, 2020)
criteria provided, single submitterVCV001072475
30.
GRCh37:
Chr12:52306899
GRCh38:
Chr12:51913115
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Benign
(Dec 31, 2019)
criteria provided, single submitterVCV000697456
31.
GRCh37:
Chr12:52306903
GRCh38:
Chr12:51913119
ACVRL1R28Wnot providedUncertain significance
(Jun 1, 2020)
criteria provided, single submitterVCV000806890
32.
GRCh37:
Chr12:52306904
GRCh38:
Chr12:51913120
ACVRL1G29fsnot provided, Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Mar 17, 2021)
criteria provided, multiple submitters, no conflictsVCV000847246
33.
GRCh37:
Chr12:52306908
GRCh38:
Chr12:51913124
ACVRL1not providedLikely benignno assertion criteria providedVCV001210058
34.
GRCh37:
Chr12:52306909
GRCh38:
Chr12:51913125
ACVRL1P30Snot provided, Haemorrhagic telangiectasia 2, Telangiectasia, hereditary hemorrhagic, type 2
Conflicting interpretations of pathogenicity
(Aug 1, 2020)
criteria provided, conflicting interpretationsVCV000161202
35.
GRCh37:
Chr12:52306920-52306921
GRCh38:
Chr12:51913136-51913137
ACVRL1C34fsHereditary hemorrhagic telangiectasia type 1Likely pathogenicno assertion criteria providedVCV000444102
36.
GRCh37:
Chr12:52306923
GRCh38:
Chr12:51913139
ACVRL1C34*Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Sep 30, 2019)
criteria provided, single submitterVCV000949903
37.
GRCh37:
Chr12:52306926
GRCh38:
Chr12:51913142
ACVRL1C36fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jul 17, 2017)
criteria provided, single submitterVCV000495052
38.
GRCh37:
Chr12:52306927
GRCh38:
Chr12:51913143
ACVRL1C36RTelangiectasia, hereditary hemorrhagic, type 2Likely pathogenic
(Feb 2, 2020)
criteria provided, single submitterVCV001066979
39.
GRCh37:
Chr12:52306932
GRCh38:
Chr12:51913148
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Likely benign
(Jan 27, 2020)
criteria provided, single submitterVCV001082795
40.
GRCh37:
Chr12:52306935-52306936
GRCh38:
Chr12:51913151-51913152
ACVRL1P39fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Apr 24, 2020)
criteria provided, single submitterVCV001072776
41.
GRCh37:
Chr12:52306942
GRCh38:
Chr12:51913158
ACVRL1C41GTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Aug 22, 2020)
criteria provided, single submitterVCV001070651
42.
GRCh37:
Chr12:52306943
GRCh38:
Chr12:51913159
ACVRL1C41YTelangiectasia, hereditary hemorrhagic, type 2Likely pathogenic
(Jan 30, 2020)
criteria provided, single submitterVCV000859439
43.
GRCh37:
Chr12:52306946-52306947
GRCh38:
Chr12:51913162-51913163
ACVRL1P44fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Nov 14, 2019)
criteria provided, single submitterVCV000962679
44.
GRCh37:
Chr12:52306952-52306953
GRCh38:
Chr12:51913168-51913169
ACVRL1C46fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Dec 7, 2018)
criteria provided, single submitterVCV001074142
45.
GRCh37:
Chr12:52306958-52306959
GRCh38:
Chr12:51913174-51913175
ACVRL1R47fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jan 1, 2018)
criteria provided, single submitterVCV000982450
46.
GRCh37:
Chr12:52306958
GRCh38:
Chr12:51913174
ACVRL1C46STelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Aug 10, 2017)
criteria provided, single submitterVCV000533345
47.
GRCh37:
Chr12:52306960-52306961
GRCh38:
Chr12:51913176-51913177
ACVRL1R47fsnot providedPathogenic
(Feb 28, 2018)
criteria provided, single submitterVCV000503681
48.
GRCh37:
Chr12:52306960-52306961
GRCh38:
Chr12:51913176-51913177
ACVRL1A49fsnot provided, Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Mar 4, 2020)
criteria provided, multiple submitters, no conflictsVCV000212805
49.
GRCh37:
Chr12:52306961
GRCh38:
Chr12:51913177
ACVRL1A49fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Mar 3, 2018)
criteria provided, single submitterVCV000568436
50.
GRCh37:
Chr12:52306961
GRCh38:
Chr12:51913177
ACVRL1R47Pnot providedPathogenic
(Nov 7, 2020)
criteria provided, single submitterVCV000381525
51.
GRCh37:
Chr12:52306964
GRCh38:
Chr12:51913180
ACVRL1G48ETelangiectasia, hereditary hemorrhagic, type 2Likely pathogenic
(Jun 28, 2018)
criteria provided, single submitterVCV000156350
52.
GRCh37:
Chr12:52306964-52306968
GRCh38:
Chr12:51913180-51913184
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(May 1, 2000)
no assertion criteria providedVCV000008247
53.
GRCh37:
Chr12:52306966
GRCh38:
Chr12:51913182
ACVRL1A49PTelangiectasia, hereditary hemorrhagic, type 2not providedno assertion providedVCV000156349
54.
GRCh37:
Chr12:52306969
GRCh38:
Chr12:51913185
ACVRL1W50RTelangiectasia, hereditary hemorrhagic, type 2Likely pathogenic
(Sep 11, 2019)
criteria provided, single submitterVCV000464760
55.
GRCh37:
Chr12:52306971
GRCh38:
Chr12:51913187
ACVRL1W50Cnot provided, Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Feb 26, 2021)
criteria provided, multiple submitters, no conflictsVCV000008246
56.
GRCh37:
Chr12:52306973
GRCh38:
Chr12:51913189
ACVRL1C51Ynot providedPathogenic
(Jan 8, 2019)
criteria provided, single submitterVCV000212797
57.
GRCh37:
Chr12:52306975
GRCh38:
Chr12:51913191
ACVRL1T52Anot providedLikely pathogenic
(Jan 31, 2020)
criteria provided, single submitterVCV000429370
58.
GRCh37:
Chr12:52307003
GRCh38:
Chr12:51913219
ACVRL1R61fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jun 26, 2016)
criteria provided, single submitterVCV000411312
59.
GRCh37:
Chr12:52307007
GRCh38:
Chr12:51913223
ACVRL1Q64fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Oct 8, 2016)
criteria provided, single submitterVCV000411306
60.
GRCh37:
Chr12:52307011
GRCh38:
Chr12:51913227
ACVRL1Q64*Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jan 29, 2019)
criteria provided, single submitterVCV000643072
61.
GRCh37:
Chr12:52307012
GRCh38:
Chr12:51913228
ACVRL1Q64Pnot providedUncertain significance
(Jun 1, 2017)
criteria provided, single submitterVCV000806891
62.
GRCh37:
Chr12:52307017
GRCh38:
Chr12:51913233
ACVRL1H66Ynot providedUncertain significance
(Jan 14, 2021)
criteria provided, single submitterVCV001216408
63.
GRCh37:
Chr12:52307020
GRCh38:
Chr12:51913236
ACVRL1R67Gnot providedLikely pathogenic
(Sep 23, 2019)
criteria provided, single submitterVCV001163055
64.
GRCh37:
Chr12:52307020
GRCh38:
Chr12:51913236
ACVRL1R67WTelangiectasia, hereditary hemorrhagic, type 2, Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasiaPathogenic
(Oct 6, 2020)
criteria provided, single submitterVCV000426010
65.
GRCh37:
Chr12:52307021
GRCh38:
Chr12:51913237
ACVRL1R67PHereditary hemorrhagic telangiectasia type 1Likely pathogenicno assertion criteria providedVCV000444100
66.
GRCh37:
Chr12:52307021
GRCh38:
Chr12:51913237
ACVRL1R67QTelangiectasia, hereditary hemorrhagic, type 2, not providedPathogenic/Likely pathogenic
(Jun 6, 2020)
criteria provided, multiple submitters, no conflictsVCV000212803
67.
GRCh37:
Chr12:52307027
GRCh38:
Chr12:51913243
ACVRL1C69YTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jun 13, 2019)
criteria provided, single submitterVCV000935121
68.
GRCh37:
Chr12:52307027
GRCh38:
Chr12:51913243
ACVRL1C69FTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Apr 10, 2019)
criteria provided, single submitterVCV000533353
69.
GRCh37:
Chr12:52307028
GRCh38:
Chr12:51913244
ACVRL1C69*Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Sep 30, 2019)
criteria provided, single submitterVCV000938281
70.
GRCh37:
Chr12:52307028
GRCh38:
Chr12:51913244
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2, not providedBenign
(Dec 1, 2020)
criteria provided, multiple submitters, no conflictsVCV000309440
71.
GRCh37:
Chr12:52307029
GRCh38:
Chr12:51913245
ACVRL1G70Rnot provided, Telangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Nov 18, 2019)
criteria provided, multiple submitters, no conflictsVCV000572085
72.
GRCh37:
Chr12:52307044
GRCh38:
Chr12:51913260
ACVRL1E75*Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jun 23, 2019)
criteria provided, single submitterVCV000933484
73.
GRCh37:
Chr12:52307046
GRCh38:
Chr12:51913262
ACVRL1E75Dnot providedUncertain significance
(Jan 20, 2020)
criteria provided, single submitterVCV001315220
74.
GRCh37:
Chr12:52307052
GRCh38:
Chr12:51913268
ACVRL1C77WTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Aug 8, 2019)
criteria provided, single submitterVCV000951985
75.
GRCh37:
Chr12:52307053-52307054
GRCh38:
Chr12:51913269-51913270
ACVRL1R80fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Oct 8, 2018)
criteria provided, single submitterVCV000644908
76.
GRCh37:
Chr12:52307054
GRCh38:
Chr12:51913270
ACVRL1R80fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jan 3, 2019)
criteria provided, single submitterVCV000838856
77.
GRCh37:
Chr12:52307057
GRCh38:
Chr12:51913273
ACVRL1G79ETelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Oct 1, 2020)
criteria provided, single submitterVCV000533350
78.
GRCh37:
Chr12:52307059
GRCh38:
Chr12:51913275
ACVRL1R80Cnot providedUncertain significance
(Apr 26, 2018)
criteria provided, single submitterVCV000617961
79.
GRCh37:
Chr12:52307072
GRCh38:
Chr12:51913288
ACVRL1F84CTelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Feb 27, 2020)
criteria provided, single submitterVCV001020566
80.
GRCh37:
Chr12:52307074
GRCh38:
Chr12:51913290
ACVRL1V85Inot providedUncertain significance
(Mar 16, 2021)
criteria provided, single submitterVCV001216542
81.
GRCh37:
Chr12:52307079
GRCh38:
Chr12:51913295
ACVRL1H87fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Jan 1, 2018)
criteria provided, single submitterVCV000982454
82.
GRCh37:
Chr12:52307080
GRCh38:
Chr12:51913296
ACVRL1H87Dnot providedUncertain significance
(Jul 30, 2019)
criteria provided, single submitterVCV001303031
83.
GRCh37:
Chr12:52307083
GRCh38:
Chr12:51913299
ACVRL1Y88DLip telangiectasia, Oral cavity telangiectasia, Telangiectasia of the skin,
Spontaneous, recurrent epistaxis
Uncertain significance
(Jan 1, 2017)
criteria provided, single submitterVCV000523311
84.
GRCh37:
Chr12:52307084
GRCh38:
Chr12:51913300
ACVRL1Y88CTelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Aug 6, 2020)
criteria provided, single submitterVCV001017571
85.
GRCh37:
Chr12:52307085
GRCh38:
Chr12:51913301
ACVRL1Y88*not providedPathogenic
(Aug 24, 2017)
criteria provided, single submitterVCV000618515
86.
GRCh37:
Chr12:52307086
GRCh38:
Chr12:51913302
ACVRL1C89GTelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Mar 24, 2018)
criteria provided, single submitterVCV000533352
87.
GRCh37:
Chr12:52307086
GRCh38:
Chr12:51913302
ACVRL1C89Rnot specifiedPathogenic
(Oct 16, 2016)
criteria provided, single submitterVCV000439381
88.
GRCh37:
Chr12:52307087
GRCh38:
Chr12:51913303
ACVRL1C89FTelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Jul 9, 2016)
criteria provided, single submitterVCV000411299
89.
GRCh37:
Chr12:52307088
GRCh38:
Chr12:51913304
ACVRL1C89WTelangiectasia, hereditary hemorrhagic, type 2Likely pathogenic
(Nov 1, 2018)
criteria provided, single submitterVCV000652880
90.
GRCh37:
Chr12:52307090
GRCh38:
Chr12:51913306
ACVRL1C90FTelangiectasia, hereditary hemorrhagic, type 2Uncertain significance
(Mar 4, 2019)
criteria provided, single submitterVCV000652184
91.
GRCh37:
Chr12:52307090
GRCh38:
Chr12:51913306
ACVRL1C90YTelangiectasia, hereditary hemorrhagic, type 2, not providedPathogenic/Likely pathogenic
(Jan 1, 2018)
criteria provided, multiple submitters, no conflictsVCV000212798
92.
GRCh37:
Chr12:52307091
GRCh38:
Chr12:51913307
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Conflicting interpretations of pathogenicity
(Oct 21, 2019)
criteria provided, conflicting interpretationsVCV000881840
93.
GRCh37:
Chr12:52307091
GRCh38:
Chr12:51913307
ACVRL1C90*Telangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Aug 27, 2018)
criteria provided, single submitterVCV000654296
94.
GRCh37:
Chr12:52307092
GRCh38:
Chr12:51913308
ACVRL1D91fsnot specifiedPathogenic
(Sep 20, 2016)
criteria provided, single submitterVCV000439378
95.
GRCh37:
Chr12:52307114
GRCh38:
Chr12:51913330
ACVRL1N98STelangiectasia, hereditary hemorrhagic, type 2, Primary pulmonary hypertension 1Uncertain significance
(Nov 21, 2018)
criteria provided, single submitterVCV000426011
96.
GRCh37:
Chr12:52307115-52307116
GRCh38:
Chr12:51913331-51913332
ACVRL1S100fsTelangiectasia, hereditary hemorrhagic, type 2Pathogenic
(Nov 1, 2019)
criteria provided, single submitterVCV000993817
97.
GRCh37:
Chr12:52307115
GRCh38:
Chr12:51913331
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Likely benign
(Jan 6, 2019)
criteria provided, single submitterVCV000700781
98.
GRCh37:
Chr12:52307115-52307119
GRCh38:
Chr12:51913331-51913335
ACVRL1V99fsnot providedPathogenic
(Mar 21, 2017)
criteria provided, single submitterVCV000426959
99.
GRCh37:
Chr12:52307123
GRCh38:
Chr12:51913339
ACVRL1L101fsnot providedLikely pathogenic
(Dec 13, 2016)
criteria provided, single submitterVCV000420920
100.
GRCh37:
Chr12:52307124
GRCh38:
Chr12:51913340
ACVRL1Telangiectasia, hereditary hemorrhagic, type 2Likely benign
(Dec 31, 2019)
criteria provided, single submitterVCV000725453
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