Canonical Allele Identifier: PA2827179467
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 391864
ClinVar RCV Id: RCV001721458 RCV001331798
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309867.1:p.Ile120Thr
CA3969503
NM_001322938.2:c.359T>C