Canonical Allele Identifier: PA2827028303
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2950820
ClinVar RCV Id: RCV003810130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu1081Asp
CA362683389
NM_001319034.2:c.3243G>C
CA362683390
NM_001319034.2:c.3243G>T