Canonical Allele Identifier: PA913191903
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 594706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.His308Gln
CA8815090
NM_000152.5:c.924C>A
CA401364060
NM_000152.5:c.924C>G