Canonical Allele Identifier: PA113466
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Leu299Arg
CA116601
NM_000152.5:c.896T>G