Canonical Allele Identifier: PA2826507090
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1334278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser111Phe
CA5689576
NM_001269039.3:c.332C>T