Allele Registry

Canonical Allele Identifier: PA916044690

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017539

RCV003556032

ClinVar Variation:

16156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351114.1:p.Arg478His	CA126236 NM_001364185.1:c.1433G>A