Canonical Allele Identifier: PA915964111
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 596014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Thr23Ala
CA8814777
NM_001079804.3:c.67A>G