Allele Registry

Canonical Allele Identifier: PA915977565

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000280379

RCV001379322

ClinVar Variation:

283227

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Arg98Pro	CA10604429 NM_001135697.3:c.293G>C