Allele Registry

Canonical Allele Identifier: PA260498

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV000030343

ClinVar Variation:

36664

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Leu365Pro	CA260497 NM_000475.5:c.1094T>C