Allele Registry

Canonical Allele Identifier: PA2825095941

Gene: SGCG HGNC NCBI

ClinVar Variation Id: 281085

HGVS (amino-acid)	Matching Registered Transcripts
NP_000222.2:p.Leu194Ser	CA6909795 NM_000231.3:c.581T>C