Canonical Allele Identifier: PA2825464287
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1722211
ClinVar RCV Id: RCV002302379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073591.1:p.Gly93Asp
CA408152002
NM_001080122.1:c.278G>A