Allele Registry

Canonical Allele Identifier: PA111429

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014341

RCV001851852

RCV003987321

ClinVar Variation:

13402

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Gln217Arg	CA256780 NM_000311.5:c.650A>G