Allele Registry

Canonical Allele Identifier: PA2828099349

Gene: NR1H3 HGNC NCBI

ClinVar RCV:

RCV000211445

ClinVar Variation:

226296

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350524.1:p.Arg310Gln	CA5973720 NM_001363595.2:c.929G>A