Canonical Allele Identifier: PA2827029921
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199910
ClinVar RCV Id: RCV000181350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Lys2343Met
CA007494
NM_001319034.2:c.7028A>T