Allele Registry

Canonical Allele Identifier: PA658706060

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000584385

RCV000635250

ClinVar Variation:

492856

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Leu381Pro	CA412546292 NM_000475.5:c.1142T>C