Canonical Allele Identifier: PA916026701
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 391864
ClinVar RCV Id: RCV001721458 RCV001331798
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309868.1:p.Ile139Thr
CA3969503
NM_001322939.2:c.416T>C