Allele Registry

Canonical Allele Identifier: PA2825464205

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014347

RCV003514300

ClinVar Variation:

13407

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073590.1:p.Thr183Ala	CA123090 NM_001080121.1:c.547A>G