Canonical Allele Identifier: PA645483468
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 338646
ClinVar RCV Id: RCV000326386 RCV000527040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Gly54Ser
CA9752018
NM_000311.5:c.160G>A