Canonical Allele Identifier: PA354653
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 218578
ClinVar RCV Id: RCV000202898 RCV000283524 RCV000644590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Pro47Ser
CA249095
NM_001271561.3:c.139C>T