Canonical Allele Identifier: PA2827179208
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 446171
ClinVar RCV Id: RCV000515451
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309866.1:p.Arg267Gly
CA365392721
NM_001322937.2:c.799A>G