Canonical Allele Identifier: PA645461902
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 357965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu2628Pro
CA051060
NM_004415.4:c.7883T>C