Canonical Allele Identifier: PA2826507187
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 830079
ClinVar RCV Id: RCV001030085 RCV001772201
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Tyr189Phe
CA378386067
NM_001269039.3:c.566A>T