Allele Registry

Canonical Allele Identifier: PA2827179862

Gene: DSE HGNC NCBI

ClinVar RCV:

RCV000436673

RCV002522675

ClinVar Variation:

392192

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309869.1:p.Arg148His	CA3969607 NM_001322940.2:c.443G>A