Allele Registry

Canonical Allele Identifier: PA915977592

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000277867

RCV000725508

RCV001122686

ClinVar Variation:

284685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Ile103Val	CA8643746 NM_001135697.3:c.307A>G