Canonical Allele Identifier: PA2827028868
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 567189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Tyr1504His
CA045899
NM_001319034.2:c.4510T>C