Canonical Allele Identifier: PA2825116281
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1495663
ClinVar RCV Id: RCV001991499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Gly29Glu
CA311093181
NM_000311.5:c.86G>A