Canonical Allele Identifier: PA2827028793
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1895478
ClinVar RCV Id: RCV002569461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser1451Arg
CA362689172
NM_001319034.2:c.4351A>C
CA362689178
NM_001319034.2:c.4353T>A
CA362689179
NM_001319034.2:c.4353T>G