Canonical Allele Identifier: PA111472
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13412
ClinVar RCV Id: RCV000014353 RCV000014354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.His187Arg
CA123096
NM_000311.5:c.560A>G