Allele Registry

Canonical Allele Identifier: PA2827938895

Gene: NR3C2 HGNC NCBI

ClinVar Allele:

23596

ClinVar RCV:

RCV000009088

ClinVar Variation:

8557

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341748.1:p.Ser693Leu	CA119732 NM_001354819.1:c.2078C>T