Canonical Allele Identifier: PA1139719582
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 862390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg2075Trp
CA047094
NM_004415.4:c.6223C>T