Canonical Allele Identifier: PA2825065863
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 660436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gly532Ser
CA8815388
NM_000152.5:c.1594G>A