Canonical Allele Identifier: PA2825464153
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13397
ClinVar RCV Id: RCV000014331 RCV000020244 RCV000014332 RCV000014333 RCV000118064 RCV000990275 RCV001262968 RCV001723566 RCV002490365 RCV003450639 RCV003313921
ClinVar Variation Id: 1562637
ClinVar RCV Id: RCV002204940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073590.1:p.Met129Val
CA123088
NM_001080121.1:c.385A>G
CA2573157041
NM_001080121.1:c.384_385delinsTG