Allele Registry

Canonical Allele Identifier: PA2826269224

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017540

ClinVar Variation:

16157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191191.1:p.Gly364Ser	CA126238 NM_001204262.2:c.1090G>A