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Links from PubMed

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(S891A +17 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+10 more
GPathogenic
RET
(V804L +17 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia
+5 more
GPathogenic
RET
(C634G +14 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic
RET
(C618G +12 more)
Single nucleotide variant
(missense variant)
Pheochromocytoma
+8 more
GPathogenic
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