Canonical Allele Identifier: PA113038
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 92465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp489Asn
CA220390
NM_000152.5:c.1465G>A