Canonical Allele Identifier: PA2825296847
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 222586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile2020Val
CA051024
NM_001008844.3:c.6058A>G