Allele Registry

Canonical Allele Identifier: PA915977432

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000294427

RCV001044076

ClinVar Variation:

286013

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Val12Met	CA8643645 NM_001135697.3:c.34G>A