Allele Registry

Canonical Allele Identifier: PA2573074962

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000636846

ClinVar Variation:

530807

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365173.1:p.Arg184Gln	CA6909702 NM_001378244.1:c.551G>A