Allele Registry

Canonical Allele Identifier: PA915977581

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000309945

RCV000485521

ClinVar Variation:

284708

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Arg98Cys	CA8643744 NM_001135697.3:c.292C>T