Allele Registry

Canonical Allele Identifier: PA915977690

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000010043

ClinVar Variation:

9436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Val175Ala	CA120425 NM_001135697.3:c.524T>C