Canonical Allele Identifier: PA2825296884
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1171370
ClinVar RCV Id: RCV001524426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Gly2048Val
CA362694107
NM_001008844.3:c.6143G>T