Canonical Allele Identifier: PA2825464481
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073592.1:p.Glu200Lys
CA256778
NM_001080123.1:c.598G>A