Canonical Allele Identifier: PA2826527461
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 338646
ClinVar RCV Id: RCV000326386 RCV000527040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Arg24Gln
CA9752018
NM_001271561.3:c.71G>A