Allele Registry

Canonical Allele Identifier: PA2826269272

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017540

ClinVar Variation:

16157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191192.1:p.Gly349Ser	CA126238 NM_001204263.2:c.1045G>A