Canonical Allele Identifier: PA2827029914
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1720208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu2338Ser
CA362694955
NM_001319034.2:c.7013T>C