Canonical Allele Identifier: PA2827168938
Gene: IDE HGNC NCBI

Linked Data

ClinVar Variation Id: 3108016
ClinVar RCV Id: RCV004397849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309724.1:p.Thr275Ser
CA377586788
NM_001322795.2:c.823A>T