Canonical Allele Identifier: PA915964935
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 663367
ClinVar RCV Id: RCV000821231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Arg881Gly
CA8815799
NM_001079804.3:c.2641A>G