Allele Registry

Canonical Allele Identifier: PA2573074961

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000271055

RCV000365766

RCV001094118

ClinVar Variation:

311480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365173.1:p.Val178Ala	CA6909699 NM_001378244.1:c.533T>C