Canonical Allele Identifier: PA112844
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 189188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg224Trp
CA274477
NM_000152.5:c.670C>T