Allele Registry

Canonical Allele Identifier: PA2826269282

Gene: NR3C1 HGNC NCBI

ClinVar Allele:

31191

ClinVar RCV:

RCV000017534

ClinVar Variation:

16152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191192.1:p.Ile417Met	CA126227 NM_001204263.2:c.1251T>G