Allele Registry

Canonical Allele Identifier: PA2826269232

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017541

ClinVar Variation:

16158

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191191.1:p.Phe422Leu	CA126240 NM_001204262.2:c.1264T>C CA361868666 NM_001204262.2:c.1266C>G CA361868667 NM_001204262.2:c.1266C>A