Canonical Allele Identifier: PA2825464226
Gene: PRNP HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073590.1:p.Glu211Gln
CA266210
NM_001080121.1:c.631G>C