Canonical Allele Identifier: PA2825295701
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 517399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala1067Val
CA362683282
NM_001008844.3:c.3200C>T