Canonical Allele Identifier: PA2825464434
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1334094
ClinVar RCV Id: RCV001809309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073592.1:p.Gly131Glu
CA408152247
NM_001080123.1:c.392G>A