Allele Registry

Canonical Allele Identifier: PA2573182350

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV002019675

ClinVar Variation:

1498501

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Arg34Ser	CA400176636 NM_001135697.3:c.100C>A