Canonical Allele Identifier: PA2827028824
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1749419
ClinVar RCV Id: RCV002349911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Leu1474Val
CA133972258
NM_001319034.2:c.4420C>G