Canonical Allele Identifier: PA2826527474
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1617003
ClinVar RCV Id: RCV002076280 RCV003883778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258490.1:p.Pro47_Ala54del
CA509567202
NM_001271561.3:c.139_162del