Allele Registry

Canonical Allele Identifier: PA2825464491

Gene: PRNP HGNC NCBI

ClinVar Allele:

94480

ClinVar RCV:

RCV000074468

ClinVar Variation:

88923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073592.1:p.Glu211Gln	CA266210 NM_001080123.1:c.631G>C