Canonical Allele Identifier: PA2827029691
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 405230
ClinVar RCV Id: RCV000461737 RCV000786122 RCV001524816 RCV002480359 RCV004000641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg2196Trp
CA051144
NM_001319034.2:c.6586C>T