Canonical Allele Identifier: PA2826527456
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1980378
ClinVar RCV Id: RCV002780237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Ala11Thr
CA9752014
NM_001271561.3:c.31G>A