Canonical Allele Identifier: PA198784
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 188479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val357Phe
CA198782
NM_000152.5:c.1069G>T