Canonical Allele Identifier: PA2827250917
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 280656
ClinVar RCV Id: RCV000379359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser3Gly
CA5689544
NM_001324336.2:c.7A>G