Allele Registry

Canonical Allele Identifier: PA2826269262

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017533

ClinVar Variation:

16151

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191192.1:p.Ile229Asn	CA126225 NM_001204263.2:c.686T>A