Canonical Allele Identifier: PA145771
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 92476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val780Ile
CA145769
NM_000152.5:c.2338G>A