Canonical Allele Identifier: PA2825116290
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 895060
ClinVar RCV Id: RCV001136928 RCV001811670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Arg48His
CA311093220
NM_000311.5:c.143G>A