Canonical Allele Identifier: PA2827029070
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Val1664Leu
CA006855
NM_001319034.2:c.4990G>C