Canonical Allele Identifier: PA658678687
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ala261Thr
CA8815016
NM_000152.5:c.781G>A