Canonical Allele Identifier: PA2825464489
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073592.1:p.Val210Ile
CA256781
NM_001080123.1:c.628G>A