Canonical Allele Identifier: PA2825296252
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Val1508Leu
CA006855
NM_001008844.3:c.4522G>C