Allele Registry

Canonical Allele Identifier: PA112362

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000011704

ClinVar Variation:

10957

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Asn440Ile	CA255628 NM_000475.5:c.1319A>T