Allele Registry

Canonical Allele Identifier: PA916039466

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000245161

RCV000313848

RCV001610587

ClinVar Variation:

256832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341748.1:p.Val180Ile	CA3100448 NM_001354819.1:c.538G>A