Allele Registry

Canonical Allele Identifier: PA2825459994

Gene: GAA HGNC NCBI

ClinVar Variation Id: 1516069

ClinVar RCV Id: RCV002048680

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073271.1:p.Ser143Ala	CA401361278 NM_001079803.3:c.427T>G