Allele Registry

Canonical Allele Identifier: PA119733

Gene: NR3C2 HGNC NCBI

ClinVar Allele:

23596

ClinVar RCV:

RCV000009088

ClinVar Variation:

8557

HGVS (amino-acid)	Matching Registered Transcripts
NP_000892.2:p.Ser810Leu	CA119732 NM_000901.5:c.2429C>T