Canonical Allele Identifier: PA2827168939
Gene: IDE HGNC NCBI

Linked Data

ClinVar Variation Id: 3108017
ClinVar RCV Id: RCV004397850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309724.1:p.Lys283Arg
CA5603610
NM_001322795.2:c.848A>G