Canonical Allele Identifier: PA1139736300
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 830079
ClinVar RCV Id: RCV001030085 RCV001772201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Tyr189Phe
CA378386067
NM_007373.4:c.566A>T