Canonical Allele Identifier: PA2826527472
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1496345
ClinVar RCV Id: RCV002019177 RCV003388076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Ala45_Gly52del
CA9752028
NM_001271561.3:c.133_156del