Canonical Allele Identifier: PA2827029669
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 222586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ile2176Val
CA051024
NM_001319034.2:c.6526A>G