Canonical Allele Identifier: PA658672636
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 453305
ClinVar RCV Id: RCV000549562
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Ser31Pro
CA509567684
NM_001271561.3:c.91T>C