Canonical Allele Identifier: PA2499302945
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1005336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898902.1:p.Ser97Asn
CA311093299
NM_183079.4:c.290G>A