Allele Registry

Canonical Allele Identifier: PA119741

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000009095

ClinVar Variation:

8564

HGVS (amino-acid)	Matching Registered Transcripts
NP_000892.2:p.Gly633Arg	CA119740 NM_000901.5:c.1897G>A CA358242773 NM_000901.5:c.1897G>C