Canonical Allele Identifier: PA2825464408
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 338646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073592.1:p.Gly54Ser
CA9752018
NM_001080123.1:c.160G>A