Canonical Allele Identifier: PA2580180006
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 2318704
ClinVar RCV Id: RCV002915098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Trp42Ser
CA408151863
NM_001271561.3:c.125G>C