Canonical Allele Identifier: PA2827029989
Gene: DSP HGNC NCBI
ClinVar RCV:
RCV001884442
ClinVar Variation:
1388205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg2383Gly
CA362695227
NM_001319034.2:c.7147C>G