ClinGen Allele Registry
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Canonical Allele Identifier:
PA123095
Gene: PRNP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000014350
RCV000020257
RCV000873683
RCV001573203
ClinVar Variation:
13409
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000302.1:p.Glu219Lys
CA123094
NM_000311.5:c.655G>A