Allele Registry

Canonical Allele Identifier: PA915977433

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000648062

RCV001288754

ClinVar Variation:

538663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Gly17Arg	CA8643683 NM_001135697.3:c.49G>A CA400176330 NM_001135697.3:c.49G>C