Canonical Allele Identifier: PA2827251357
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1334278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ser111Phe
CA5689576
NM_001324337.2:c.332C>T