Canonical Allele Identifier: PA916052480
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13397
ClinVar Variation Id: 1562637
ClinVar RCV Id: RCV002204940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898902.1:p.Met129Val
CA123088
NM_183079.4:c.385A>G
CA2573157041
NM_183079.4:c.384_385delinsTG