Canonical Allele Identifier: PA2825297106
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1052918
ClinVar RCV Id: RCV001361187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg2192Gly
CA362695019
NM_001008844.3:c.6574C>G