Allele Registry

Canonical Allele Identifier: PA2826269302

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017539

RCV003556032

ClinVar Variation:

16156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191193.1:p.Arg142His	CA126236 NM_001204264.2:c.425G>A