Allele Registry

Canonical Allele Identifier: PA112433

Gene: NR0B1 HGNC NCBI

ClinVar Allele:

26003

ClinVar RCV:

RCV000011711

ClinVar Variation:

10964

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Lys382Asn	CA255633 NM_000475.5:c.1146G>T CA412546273 NM_000475.5:c.1146G>C