Allele Registry

Canonical Allele Identifier: PA916052535

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014340

RCV000644586

RCV001551488

ClinVar Variation:

13401

HGVS (amino-acid)	Matching Registered Transcripts
NP_898902.1:p.Phe198Ser	CA256779 NM_183079.4:c.593T>C