Canonical Allele Identifier: PA2825296065
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Trp1360Arg
CA362689603
NM_001008844.3:c.4078T>A
CA362689605
NM_001008844.3:c.4078T>C