Allele Registry

Canonical Allele Identifier: PA112453

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000011720

ClinVar Variation:

10973

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Tyr380Asp	CA255639 NM_000475.5:c.1138T>G