Allele Registry

Canonical Allele Identifier: PA916044700

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017538

ClinVar Variation:

16155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351114.1:p.Leu774Pro	CA126234 NM_001364185.1:c.2321T>C