Allele Registry

Canonical Allele Identifier: PA2828132237

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017540

ClinVar Variation:

16157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351112.1:p.Gly680Ser	CA126238 NM_001364183.2:c.2038G>A