Allele Registry

Canonical Allele Identifier: PA263241

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000049288

ClinVar Variation:

55874

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Arg425Ile	CA263240 NM_000475.5:c.1274G>T