Canonical Allele Identifier: PA2830409786
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 2207104
ClinVar RCV Id: RCV002641730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898902.1:p.Arg37Gln
CA408151643
NM_183079.4:c.110G>A