Canonical Allele Identifier: PA2827028794
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2071274
ClinVar RCV Id: RCV002949267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser1451Thr
CA362689175
NM_001319034.2:c.4352G>C