Canonical Allele Identifier: PA2825296866
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1002980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile2038Thr
CA362694045
NM_001008844.3:c.6113T>C