Allele Registry

Canonical Allele Identifier: PA915977499

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000384383

RCV003137892

ClinVar Variation:

286025

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Leu66His	CA501057 NM_001135697.3:c.197T>A