Canonical Allele Identifier: PA645481796
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 285589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ile468Phe
CA10605170
NM_000152.5:c.1402A>T