Canonical Allele Identifier: PA2825065639
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1388042
ClinVar RCV Id: RCV001875730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ala426Thr
CA401365331
NM_000152.5:c.1276G>A