Canonical Allele Identifier: PA2825461793
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 660436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Gly532Ser
CA8815388
NM_001079803.3:c.1594G>A