Canonical Allele Identifier: PA2827180313
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 391864
ClinVar RCV Id: RCV001721458 RCV001331798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309872.1:p.Ile120Thr
CA3969503
NM_001322943.2:c.359T>C