Canonical Allele Identifier: PA658669902
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465900
ClinVar RCV Id: RCV000542834 RCV001177353 RCV001811049 RCV002358509 RCV003999173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1932Cys
CA045687
NM_004415.4:c.5794C>T