Canonical Allele Identifier: PA2825460898
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1346780
ClinVar RCV Id: RCV002030183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Gly335Trp
CA401364543
NM_001079803.3:c.1003G>T