Canonical Allele Identifier: PA915964822
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 426278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Arg702His
CA8815610
NM_001079804.3:c.2105G>A