Allele Registry

Canonical Allele Identifier: PA112333

Gene: NR0B1 HGNC NCBI

ClinVar Allele:

25991

ClinVar RCV:

RCV000011699

RCV001851797

ClinVar Variation:

10952

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Arg267Pro	CA255621 NM_000475.5:c.800G>C