Canonical Allele Identifier: PA2825442725
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2189632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Ala495Val
CA401366956
NM_001079804.3:c.1484C>T