Canonical Allele Identifier: PA2827028355
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1018579
ClinVar RCV Id: RCV001317906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg1125del
CA828077130
NM_001319034.2:c.3374_3376del