Allele Registry

Canonical Allele Identifier: PA111396

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000020248

RCV001200144

RCV001214652

ClinVar Variation:

39359

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Asp178Asn	CA261110 NM_000311.5:c.532G>A