Allele Registry

Canonical Allele Identifier: PA123093

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014348

RCV000020247

RCV000644585

RCV001580052

RCV001725931

ClinVar Variation:

13408

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Asn171Ser	CA123092 NM_000311.5:c.512A>G