Allele Registry

Canonical Allele Identifier: PA256787

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014356

ClinVar Variation:

13414

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Ala133Val	CA256786 NM_000311.5:c.398C>T