Canonical Allele Identifier: PA2827028402
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1171817

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu1168Asp
CA362684214
NM_001319034.2:c.3504G>T
CA362684215
NM_001319034.2:c.3504G>C