Allele Registry

Canonical Allele Identifier: PA2828527852

Gene: DSE HGNC NCBI

ClinVar RCV:

RCV000522074

RCV001490971

ClinVar Variation:

450138

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361450.1:p.Val288Met	CA3969726 NM_001374521.1:c.862G>A