Canonical Allele Identifier: PA915964407
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Ala261Thr
CA8815016
NM_001079804.3:c.781G>A