Canonical Allele Identifier: PA658801217
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 497169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ala25Val
CA8814782
NM_000152.5:c.74C>T