Canonical Allele Identifier: PA2825296568
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2933096
ClinVar RCV Id: RCV003790214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Val1789Ala
CA362692375
NM_001008844.3:c.5366T>C