Allele Registry

Canonical Allele Identifier: PA2825095891

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000636846

ClinVar Variation:

530807

HGVS (amino-acid)	Matching Registered Transcripts
NP_000222.2:p.Arg166Gln	CA6909702 NM_000231.3:c.497G>A