Canonical Allele Identifier: PA2825065089
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 842132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg168Trp
CA8814882
NM_000152.5:c.502C>T