Allele Registry

Canonical Allele Identifier: PA2826269329

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017534

ClinVar Variation:

16152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191193.1:p.Ile412Met	CA126227 NM_001204264.2:c.1236T>G