Canonical Allele Identifier: PA2827028841
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg1489Cys
CA045687
NM_001319034.2:c.4465C>T