Canonical Allele Identifier: PA2825296860
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2945721
ClinVar RCV Id: RCV003803815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser2033Pro
CA362694011
NM_001008844.3:c.6097T>C