Allele Registry

Canonical Allele Identifier: PA112378

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000011716

ClinVar Variation:

10969

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Ile439Ser	CA255637 NM_000475.5:c.1316T>G