Canonical Allele Identifier: PA916052550
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 88922
ClinVar RCV Id: RCV000074467 RCV001854271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898902.1:p.Glu211Asp
CA266208
NM_183079.4:c.633G>C
CA408152780
NM_183079.4:c.633G>T