Allele Registry

Canonical Allele Identifier: PA2825065132

Gene: GAA HGNC NCBI

ClinVar RCV:

RCV001915038

ClinVar Variation:

1398409

HGVS (amino-acid)	Matching Registered Transcripts
NP_000143.2:p.Tyr191Asp	CA401362120 NM_000152.5:c.571T>G