Canonical Allele Identifier: PA2826527470
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 453304
ClinVar RCV Id: RCV000536485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Ala37Thr
CA9752025
NM_001271561.3:c.109G>A