Allele Registry

Canonical Allele Identifier: PA2825461811

Gene: GAA HGNC NCBI

ClinVar Variation Id: 1412665

ClinVar RCV Id: RCV001943251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073271.1:p.Tyr543Cys	CA401367360 NM_001079803.3:c.1628A>G