Allele Registry

Canonical Allele Identifier: PA1139670650

Gene: GAA HGNC NCBI

ClinVar RCV:

RCV001279297

ClinVar Variation:

991137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073272.1:p.Asp227Tyr	CA401362561 NM_001079804.3:c.679G>T