Canonical Allele Identifier: PA111531
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13403
ClinVar RCV Id: RCV000014342 RCV000532969 RCV002476962 RCV004018625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Val210Ile
CA256781
NM_000311.5:c.628G>A