Allele Registry

Canonical Allele Identifier: PA123098

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014355

ClinVar Variation:

13413

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Pro105Thr	CA123097 NM_000311.5:c.313C>A