Allele Registry

Canonical Allele Identifier: PA2828132254

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017538

ClinVar Variation:

16155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351112.1:p.Leu774Pro	CA126234 NM_001364183.2:c.2321T>C