Allele Registry

Canonical Allele Identifier: PA916052558

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014350

RCV000020257

RCV000873683

RCV001573203

ClinVar Variation:

13409

HGVS (amino-acid)	Matching Registered Transcripts
NP_898902.1:p.Glu219Lys	CA123094 NM_183079.4:c.655G>A