Canonical Allele Identifier: PA2827028761
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1500153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Tyr1428Asp
CA045361
NM_001319034.2:c.4282T>G