Allele Registry

Canonical Allele Identifier: PA2825096037

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000002086

RCV000078408

ClinVar Variation:

2009

HGVS (amino-acid)	Matching Registered Transcripts
NP_000222.2:p.Glu263Lys	CA220515 NM_000231.3:c.787G>A