Allele Registry

Canonical Allele Identifier: PA645492919

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000245161

RCV000313848

RCV001610587

ClinVar Variation:

256832

HGVS (amino-acid)	Matching Registered Transcripts
NP_000892.2:p.Val180Ile	CA3100448 NM_000901.5:c.538G>A