Allele Registry

Canonical Allele Identifier: PA112443

Gene: NR0B1 HGNC NCBI

ClinVar Allele:

26004

ClinVar RCV:

RCV000011712

ClinVar Variation:

10965

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Trp291Cys	CA255634 NM_000475.5:c.873G>C CA412547486 NM_000475.5:c.873G>T