Canonical Allele Identifier: PA2825116297
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1705547
ClinVar RCV Id: RCV002283861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.His69Leu
CA408151849
NM_000311.5:c.206A>T