Canonical Allele Identifier: PA111459
Gene: PRNP HGNC NCBI
ClinVar RCV:
RCV000074468
ClinVar Variation:
88923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Glu211Gln
CA266210
NM_000311.5:c.631G>C