Allele Registry

Canonical Allele Identifier: PA916052455

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014355

ClinVar Variation:

13413

HGVS (amino-acid)	Matching Registered Transcripts
NP_898902.1:p.Pro105Thr	CA123097 NM_183079.4:c.313C>A