Canonical Allele Identifier: PA645500838
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 338647
ClinVar RCV Id: RCV000383267 RCV000874283 RCV001580001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Ser39Pro
CA9752026
NM_001271561.3:c.115T>C