Allele Registry

Canonical Allele Identifier: PA2826269112

Gene: NR3C1 HGNC NCBI

ClinVar Allele:

31194

ClinVar RCV:

RCV000017538

ClinVar Variation:

16155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191189.1:p.Leu684Pro	CA126234 NM_001204260.2:c.2051T>C