Canonical Allele Identifier: PA2827179862
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_001309869.1:p.Arg148His
CA3969607
NM_001322940.2:c.443G>A