Canonical Allele Identifier: PA2825464480
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13401
ClinVar RCV Id: RCV000014340 RCV000644586 RCV001551488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073592.1:p.Phe198Ser
CA256779
NM_001080123.1:c.593T>C