Canonical Allele Identifier: PA2825116310
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1005336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Ser97Asn
CA311093299
NM_000311.5:c.290G>A