Canonical Allele Identifier: PA2825296893
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2025955
ClinVar RCV Id: RCV002858247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala2056Ser
CA051243
NM_001008844.3:c.6166G>T