Canonical Allele Identifier: PA2827179615
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 452829
ClinVar RCV Id: RCV000520971 RCV001853691 RCV004023623
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309867.1:p.Arg723Gln
CA3969774
NM_001322938.2:c.2168G>A