Canonical Allele Identifier: PA266209
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 88922
ClinVar RCV Id: RCV000074467 RCV001854271
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Glu211Asp
CA266208
NM_000311.5:c.633G>C
CA408152780
NM_000311.5:c.633G>T