Allele Registry

Canonical Allele Identifier: PA916052532

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014353

RCV000014354

ClinVar Variation:

13412

HGVS (amino-acid)	Matching Registered Transcripts
NP_898902.1:p.His187Arg	CA123096 NM_183079.4:c.560A>G