Canonical Allele Identifier: PA2825464491
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 88923
ClinVar RCV Id: RCV000074468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073592.1:p.Glu211Gln
CA266210
NM_001080123.1:c.631G>C