Allele Registry

Canonical Allele Identifier: PA117538

Gene: NR0B2 HGNC NCBI

ClinVar RCV:

RCV000005760

RCV002247254

ClinVar Variation:

5427

HGVS (amino-acid)	Matching Registered Transcripts
NP_068804.1:p.Ala195Ser	CA117537 NM_021969.3:c.583G>T