Canonical Allele Identifier: PA111496
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13395
ClinVar RCV Id: RCV000014329 RCV001203438 RCV001269667 RCV001813741 RCV001642224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000302.1:p.Pro102Leu
CA256774
NM_000311.5:c.305C>T