Allele Registry

Canonical Allele Identifier: PA112413

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000011718

ClinVar Variation:

10971

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Leu381His	CA255638 NM_000475.5:c.1142T>A