Canonical Allele Identifier: PA2827251040
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1746510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Leu176Ile
CA378385834
NM_001324336.2:c.526T>A