Allele Registry

Canonical Allele Identifier: PA111468

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014351

RCV001348311

ClinVar Variation:

13410

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Gly131Val	CA256784 NM_000311.5:c.392G>T