Allele Registry

Canonical Allele Identifier: PA119758

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000009103

ClinVar Variation:

8572

HGVS (amino-acid)	Matching Registered Transcripts
NP_000892.2:p.Glu972Gly	CA119757 NM_000901.5:c.2915A>G