Canonical Allele Identifier: PA2825461718
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2189632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Ala495Val
CA401366956
NM_001079803.3:c.1484C>T