Canonical Allele Identifier: PA2825294648
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1026944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala261Thr
CA133954649
NM_001008844.3:c.781G>A