Canonical Allele Identifier: PA2827028881
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923470
ClinVar RCV Id: RCV001184179 RCV003770040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Trp1516Arg
CA362689603
NM_001319034.2:c.4546T>A
CA362689605
NM_001319034.2:c.4546T>C