Canonical Allele Identifier: PA2573176568
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1355553
ClinVar RCV Id: RCV001866976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Ala261Pro
CA401363450
NM_001079804.3:c.781G>C