Allele Registry

Canonical Allele Identifier: PA111506

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014343

RCV000190750

ClinVar Variation:

13404

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Pro105Leu	CA204782 NM_000311.5:c.314C>T