Allele Registry

Canonical Allele Identifier: PA119739

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000009094

ClinVar Variation:

8563

HGVS (amino-acid)	Matching Registered Transcripts
NP_000892.2:p.Gln776Arg	CA119738 NM_000901.5:c.2327A>G