Canonical Allele Identifier: PA2825065537
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 843921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr378Cys
CA294892229
NM_000152.5:c.1133A>G