Allele Registry

Canonical Allele Identifier: PA916044698

Gene: NR3C1 HGNC NCBI

ClinVar Allele:

31188

ClinVar RCV:

RCV000017531

ClinVar Variation:

16149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351114.1:p.Leu754Phe	CA126221 NM_001364185.1:c.2262A>T CA361868551 NM_001364185.1:c.2262A>C