Canonical Allele Identifier: PA2825066501
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 663449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Glu866Asp
CA401326321
NM_000152.5:c.2598A>C
CA401326323
NM_000152.5:c.2598A>T