Canonical Allele Identifier: PA2825296880
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923617
ClinVar RCV Id: RCV001184444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser2045Thr
CA362694087
NM_001008844.3:c.6134G>C