Allele Registry

Canonical Allele Identifier: PA2827179467

Gene: DSE HGNC NCBI

ClinVar RCV:

RCV001331798

RCV001721458

ClinVar Variation:

391864

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