Canonical Allele Identifier: PA2827029987
Gene: DSP HGNC NCBI
ClinVar RCV:
RCV001989435
ClinVar Variation:
1494560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg2383Ser
CA362695226
NM_001319034.2:c.7147C>A