Canonical Allele Identifier: PA916026703
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 392192
ClinVar RCV Id: RCV000436673 RCV002522675
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309868.1:p.Arg354His
CA3969607
NM_001322939.2:c.1061G>A