Canonical Allele Identifier: PA916052539
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13411
ClinVar RCV Id: RCV000014352 RCV001851853 RCV001823096 RCV002468968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898902.1:p.Arg208His
CA256785
NM_183079.4:c.623G>A