Allele Registry

Canonical Allele Identifier: PA2829622538

Gene: NR1H3 HGNC NCBI

ClinVar RCV:

RCV000211445

ClinVar Variation:

226296

HGVS (amino-acid)	Matching Registered Transcripts
NP_005684.2:p.Arg415Gln	CA5973720 NM_005693.3:c.1244G>A