Allele Registry

Canonical Allele Identifier: PA2573176601

Gene: GAA HGNC NCBI

ClinVar Variation Id: 1361550

ClinVar RCV Id: RCV001911834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073272.1:p.Pro326Ser	CA401364442 NM_001079804.3:c.976C>T