Allele Registry

Canonical Allele Identifier: PA2825740048

Gene: NR1H3 HGNC NCBI

ClinVar RCV:

RCV000211445

ClinVar Variation:

226296

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123573.1:p.Arg355Gln	CA5973720 NM_001130101.3:c.1064G>A