Canonical Allele Identifier: PA2826343197
Gene: NR1H3 HGNC NCBI
ClinVar RCV:
RCV000211445
ClinVar Variation:
226296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001238863.1:p.Arg421Gln
CA5973720
NM_001251934.2:c.1262G>A