Canonical Allele Identifier: PA2825297093
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1720208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu2182Ser
CA362694955
NM_001008844.3:c.6545T>C