Canonical Allele Identifier: PA2825464474
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073592.1:p.His187Arg
CA123096
NM_001080123.1:c.560A>G