Canonical Allele Identifier: PA916052518
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 13408
ClinVar RCV Id: RCV000014348 RCV000020247 RCV000644585 RCV001580052 RCV001725931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898902.1:p.Asn171Ser
CA123092
NM_183079.4:c.512A>G