Allele Registry

Canonical Allele Identifier: PA111481

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014345

RCV000990277

RCV002496357

ClinVar Variation:

13406

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Met232Arg	CA256783 NM_000311.5:c.695T>G