Canonical Allele Identifier: PA658801340
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 526538
ClinVar RCV Id: RCV000631088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val921Phe
CA401327245
NM_000152.5:c.2761G>T