Allele Registry

Canonical Allele Identifier: PA256777

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014330

RCV000623716

RCV003627888

ClinVar Variation:

13396

2815837

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Ala117Val	CA256776 NM_000311.5:c.350C>T CA2739277062 NM_000311.5:c.350_351delinsTG