Allele Registry

Canonical Allele Identifier: PA2825464226

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000074468

ClinVar Variation:

88923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073590.1:p.Glu211Gln	CA266210 NM_001080121.1:c.631G>C