Allele Registry

Canonical Allele Identifier: PA2826269236

Gene: NR3C1 HGNC NCBI

ClinVar Allele:

31188

ClinVar RCV:

RCV000017531

ClinVar Variation:

16149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191191.1:p.Leu438Phe	CA126221 NM_001204262.2:c.1314A>T CA361868551 NM_001204262.2:c.1314A>C