Canonical Allele Identifier: PA2827250946
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766489
ClinVar RCV Id: RCV002371530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser31Phe
CA378381239
NM_001324336.2:c.92C>T