Allele Registry

Canonical Allele Identifier: PA2828751422

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000271055

RCV000365766

RCV001094118

ClinVar Variation:

311480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365175.1:p.Val160Ala	CA6909699 NM_001378246.1:c.479T>C