Canonical Allele Identifier: PA645507247
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_037484.1:p.Ile120Thr
CA3969503
NM_013352.4:c.359T>C