Allele Registry

Canonical Allele Identifier: PA2826269004

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017535

ClinVar Variation:

16153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191188.1:p.Val486Ala	CA126229 NM_001204259.2:c.1457T>C