Canonical Allele Identifier: PA2580311552
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1749419
ClinVar RCV Id: RCV002349911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu1917Val
CA133972258
NM_004415.4:c.5749C>G