Canonical Allele Identifier: PA891858009
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 567189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Tyr1947His
CA045899
NM_004415.4:c.5839T>C