Allele Registry

Canonical Allele Identifier: PA2826269169

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017535

ClinVar Variation:

16153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191190.1:p.Val474Ala	CA126229 NM_001204261.2:c.1421T>C