Canonical Allele Identifier: PA111448
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13398
ClinVar RCV Id: RCV000014334 RCV000014335 RCV000644587 RCV001310451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Glu200Lys
CA256778
NM_000311.5:c.598G>A