Canonical Allele Identifier: PA645481751
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 284865
ClinVar RCV Id: RCV000343108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp404Val
CA10604928
NM_000152.5:c.1211A>T