Allele Registry

Canonical Allele Identifier: PA123100

Gene: PRNP HGNC NCBI

ClinVar RCV:

RCV000014358

ClinVar Variation:

13416

HGVS (amino-acid)	Matching Registered Transcripts
NP_000302.1:p.Gly127Val	CA123099 NM_000311.5:c.380G>T