ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825464203
Gene: PRNP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13405
ClinVar RCV Id:
RCV000014344
RCV000020249
RCV001212635
RCV001807726
RCV002476963
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073590.1:p.Val180Ile
CA256782
NM_001080121.1:c.538G>A