Canonical Allele Identifier: PA891845696
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 566063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val400Ile
CA8815232
NM_000152.5:c.1198G>A