Canonical Allele Identifier: PA2827028887
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2140517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr1520Ala
CA362689630
NM_001319034.2:c.4558A>G