Allele Registry

Canonical Allele Identifier: PA2825096065

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000002083

RCV001090241

ClinVar Variation:

2006

HGVS (amino-acid)	Matching Registered Transcripts
NP_000222.2:p.Cys283Tyr	CA339932 NM_000231.3:c.848G>A