Canonical Allele Identifier: PA2827029688
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1002980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ile2194Thr
CA362694045
NM_001319034.2:c.6581T>C