Canonical Allele Identifier: PA913191902
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 595995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gln124Glu
CA401360930
NM_000152.5:c.370C>G