Allele Registry

Canonical Allele Identifier: PA2825083996

Gene: NR3C1 HGNC NCBI

ClinVar Allele:

31188

ClinVar RCV:

RCV000017531

ClinVar Variation:

16149

HGVS (amino-acid)	Matching Registered Transcripts
NP_000167.1:p.Leu753Phe	CA126221 NM_000176.3:c.2259A>T CA361868551 NM_000176.3:c.2259A>C