Canonical Allele Identifier: PA2826507179
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1746510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Leu176Ile
CA378385834
NM_001269039.3:c.526T>A