Canonical Allele Identifier: PA2825066356
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1005758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr766Asn
CA294856634
NM_000152.5:c.2296T>A