Allele Registry

Canonical Allele Identifier: PA2827179583

Gene: DSE HGNC NCBI

ClinVar RCV:

RCV000522074

RCV001490971

ClinVar Variation:

450138

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309867.1:p.Val633Met	CA3969726 NM_001322938.2:c.1897G>A