Allele Registry

Canonical Allele Identifier: PA101196

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017541

ClinVar Variation:

16158

HGVS (amino-acid)	Matching Registered Transcripts
NP_000167.1:p.Phe737Leu	CA126240 NM_000176.3:c.2209T>C CA361868666 NM_000176.3:c.2211C>G CA361868667 NM_000176.3:c.2211C>A