Canonical Allele Identifier: PA2825460821
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1010798
ClinVar RCV Id: RCV001308498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Asp319Asn
CA401364287
NM_001079803.3:c.955G>A