Allele Registry

Canonical Allele Identifier: PA916026711

Gene: DSE HGNC NCBI

ClinVar RCV:

RCV000522074

RCV001490971

ClinVar Variation:

450138

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309868.1:p.Val652Met	CA3969726 NM_001322939.2:c.1954G>A