Canonical Allele Identifier: PA2825460558
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Ala261Thr
CA8815016
NM_001079803.3:c.781G>A