Canonical Allele Identifier: PA645481862
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 370146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser619Asn
CA8815500
NM_000152.5:c.1856G>A