Allele Registry

Canonical Allele Identifier: PA2573100820

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV001809309

ClinVar Variation:

1334094

HGVS (amino-acid)	Matching Registered Transcripts
NP_898902.1:p.Gly131Glu	CA408152247 NM_183079.4:c.392G>A