Canonical Allele Identifier: PA2827028398
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3070090
ClinVar RCV Id: RCV004010122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Lys1165Met
CA362684191
NM_001319034.2:c.3494A>T