Canonical Allele Identifier: PA2825295799
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1000822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Trp1155Cys
CA362684119
NM_001008844.3:c.3465G>T
CA362684121
NM_001008844.3:c.3465G>C