Canonical Allele Identifier: PA645481964
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 284886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.His799Tyr
CA8815726
NM_000152.5:c.2395C>T