Canonical Allele Identifier: PA2825297108
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 178962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser2193Thr
CA007514
NM_001008844.3:c.6577T>A