Canonical Allele Identifier: PA658801266
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 497377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val442Met
CA8815262
NM_000152.5:c.1324G>A