Allele Registry

Canonical Allele Identifier: PA2826268946

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017538

ClinVar Variation:

16155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191187.1:p.Leu747Pro	CA126234 NM_001204258.1:c.2240T>C