Allele Registry

Canonical Allele Identifier: PA121281

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000011725

RCV002496328

ClinVar Variation:

10978

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Trp105Cys	CA121280 NM_000475.5:c.315G>C CA412549018 NM_000475.5:c.315G>T