Canonical Allele Identifier: PA2825065799
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2189632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ala495Val
CA401366956
NM_000152.5:c.1484C>T