Canonical Allele Identifier: PA2825460689
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 498117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Asn290Asp
CA8815078
NM_001079803.3:c.868A>G