Allele Registry

Canonical Allele Identifier: PA260500

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000030344

ClinVar Variation:

36665

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Leu381Phe	CA260499 NM_000475.5:c.1141C>T