Canonical Allele Identifier: PA916026722
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 446171
ClinVar RCV Id: RCV000515451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309870.1:p.Arg80Gly
CA365392721
NM_001322941.2:c.238A>G