Canonical Allele Identifier: PA658655368
Gene: DSE HGNC NCBI

Linked Data

ClinVar Variation Id: 446171
ClinVar RCV Id: RCV000515451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037484.1:p.Arg267Gly
CA365392721
NM_013352.4:c.799A>G