Canonical Allele Identifier: PA2825461770
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1506038
ClinVar RCV Id: RCV002035896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Pro522Leu
CA401367210
NM_001079803.3:c.1565C>T