Canonical Allele Identifier: PA111516
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13405
ClinVar RCV Id: RCV000014344 RCV000020249 RCV001212635 RCV001807726 RCV002476963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Val180Ile
CA256782
NM_000311.5:c.538G>A