Allele Registry

Canonical Allele Identifier: PA2825464142

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014355

ClinVar Variation:

13413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073590.1:p.Pro105Thr	CA123097 NM_001080121.1:c.313C>A