Allele Registry

Canonical Allele Identifier: PA913196699

Gene: NR0B2 HGNC NCBI

ClinVar RCV:

RCV000730964

RCV002067111

ClinVar Variation:

595423

HGVS (amino-acid)	Matching Registered Transcripts
NP_068804.1:p.Gly171Ala	CA709629 NM_021969.3:c.512G>C