Canonical Allele Identifier: PA915964352
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 189065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Gly219Arg
CA274334
NM_001079804.3:c.655G>A
CA401362459
NM_001079804.3:c.655G>C