Allele Registry

Canonical Allele Identifier: PA915977456

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000531212

ClinVar Variation:

471339

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Pro30Ser	CA400176582 NM_001135697.3:c.88C>T