Allele Registry

Canonical Allele Identifier: PA119743

Gene: NR3C2 HGNC NCBI

ClinVar Allele:

23604

ClinVar RCV:

RCV000009096

ClinVar Variation:

8565

HGVS (amino-acid)	Matching Registered Transcripts
NP_000892.2:p.Leu979Pro	CA119742 NM_000901.5:c.2936T>C