Canonical Allele Identifier: PA645500845
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 338648
ClinVar RCV Id: RCV000340924 RCV000644591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Thr53Ala
CA9752040
NM_001271561.3:c.157A>G