Allele Registry

Canonical Allele Identifier: PA645492092

Gene: NR1H3 HGNC NCBI

ClinVar RCV:

RCV000211445

ClinVar Variation:

226296

HGVS (amino-acid)	Matching Registered Transcripts
NP_001238864.1:p.Arg421Gln	CA5973720 NM_001251935.2:c.1262G>A