Allele Registry

Canonical Allele Identifier: PA2827179157

Gene: DSE HGNC NCBI

ClinVar RCV:

RCV003064889

RCV003250725

ClinVar Variation:

2145164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309866.1:p.Gln57His	CA365534208 NM_001322937.2:c.171G>C CA365534209 NM_001322937.2:c.171G>T