Canonical Allele Identifier: PA658669732
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1113Gln
CA037833
NM_004415.4:c.3338G>A