Allele Registry

Canonical Allele Identifier: PA2826269105

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017534

ClinVar Variation:

16152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191189.1:p.Ile658Met	CA126227 NM_001204260.2:c.1974T>G