Allele Registry

Canonical Allele Identifier: PA112405

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000011723

RCV003764556

ClinVar Variation:

10976

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Leu297Pro	CA255642 NM_000475.5:c.890T>C