Allele Registry

Canonical Allele Identifier: PA3057313703

Gene: NR0B1 HGNC NCBI

ClinVar RCV:

RCV004800219

ClinVar Variation:

3385083

HGVS (amino-acid)	Matching Registered Transcripts
NP_000466.2:p.Asn440Ser	CA327974104 NM_000475.5:c.1319A>G