Canonical Allele Identifier: PA2825460992
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1176696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Val357Ile
CA8815138
NM_001079803.3:c.1069G>A