Allele Registry

Canonical Allele Identifier: PA658665488

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000531212

ClinVar Variation:

471339

HGVS (amino-acid)	Matching Registered Transcripts
NP_000014.1:p.Pro30Ser	CA400176582 NM_000023.3:c.88C>T