Allele Registry

Canonical Allele Identifier: PA916026701

Gene: DSE HGNC NCBI

ClinVar Allele:

368821

ClinVar RCV:

RCV001331798

RCV001721458

ClinVar Variation:

391864

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309868.1:p.Ile139Thr	CA3969503 NM_001322939.2:c.416T>C