Allele Registry

Canonical Allele Identifier: PA1139744609

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000002086

RCV000078408

ClinVar Variation:

2009

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365173.1:p.Glu281Lys	CA220515 NM_001378244.1:c.841G>A