Canonical Allele Identifier: PA891845734
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 571521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp741Asn
CA8815660
NM_000152.5:c.2221G>A