Allele Registry

Canonical Allele Identifier: PA2828132067

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017538

ClinVar Variation:

16155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351110.1:p.Leu773Pro	CA126234 NM_001364181.2:c.2318T>C