Canonical Allele Identifier: PA2827028358
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1730749
ClinVar RCV Id: RCV002451758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg1125Gly
CA037946
NM_001319034.2:c.3373A>G