Allele Registry

Canonical Allele Identifier: PA2826269177

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017540

ClinVar Variation:

16157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191190.1:p.Gly582Ser	CA126238 NM_001204261.2:c.1744G>A