Allele Registry

Canonical Allele Identifier: PA2826018226

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000009088

ClinVar Variation:

8557

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159576.1:p.Ser693Leu	CA119732 NM_001166104.2:c.2078C>T