Canonical Allele Identifier: PA2825444192
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2049020
ClinVar RCV Id: RCV002909486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Gln902Arg
CA401326908
NM_001079804.3:c.2705A>G