Allele Registry

Canonical Allele Identifier: PA2826268928

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017540

ClinVar Variation:

16157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191187.1:p.Gly653Ser	CA126238 NM_001204258.1:c.1957G>A