Allele Registry

Canonical Allele Identifier: PA2828751426

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000636846

ClinVar Variation:

530807

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365175.1:p.Arg166Gln	CA6909702 NM_001378246.1:c.497G>A