Allele Registry

Canonical Allele Identifier: PA256789

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014357

RCV003319302

ClinVar Variation:

13415

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Pro105Ser	CA256788 NM_000311.5:c.313C>T