Canonical Allele Identifier: PA2827029928
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1052918
ClinVar RCV Id: RCV001361187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg2348Gly
CA362695019
NM_001319034.2:c.7042C>G