Canonical Allele Identifier: PA2826527454
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1556415
ClinVar RCV Id: RCV002187888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Gly10Arg
CA9752013
NM_001271561.3:c.28G>A
CA509567591
NM_001271561.3:c.28G>C