Canonical Allele Identifier: PA2825116285
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 899178
ClinVar RCV Id: RCV001143502 RCV001361599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Pro39Leu
CA9752012
NM_000311.5:c.116C>T