NM_054027.6(ANKH):c.*2113del AND Chondrocalcinosis
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000335338.5
Allele description [Variation Report for NM_054027.6(ANKH):c.*2113del]
NM_054027.6(ANKH):c.*2113del
Condition(s)
- Name:
- Chondrocalcinosis
- Identifiers:
- MONDO: MONDO:0001314; MedGen: C0553730; Human Phenotype Ontology: HP:0000934
-
transmembrane protein PVRIG isoform X2 [Rattus norvegicus]
transmembrane protein PVRIG isoform X2 [Rattus norvegicus]gi|564378630|ref|XP_006249094.1|Protein
-
DB335303 TCOLN2 Homo sapiens cDNA clone TCOLN2000118 3', mRNA sequence
DB335303 TCOLN2 Homo sapiens cDNA clone TCOLN2000118 3', mRNA sequencegi|83080887|gnl|dbEST|34196277|dbj| 303.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Aug 25, 2024