Allele Registry

Canonical Allele Identifier: PA2825464469

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000020248

RCV001200144

RCV001214652

ClinVar Variation:

39359

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073592.1:p.Asp178Asn	CA261110 NM_001080123.1:c.532G>A