Canonical Allele Identifier: PA2827168847
Gene: IDE HGNC NCBI

Linked Data

ClinVar Variation Id: 3108016
ClinVar RCV Id: RCV004397849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309722.1:p.Thr316Ser
CA377586788
NM_001322793.2:c.946A>T