Canonical Allele Identifier: PA2825460780
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2729477
ClinVar RCV Id: RCV003504363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Gly309Trp
CA401364062
NM_001079803.3:c.925G>T