Allele Registry

Canonical Allele Identifier: PA2826269152

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017532

RCV000345541

RCV002054445

ClinVar Variation:

16150

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191190.1:p.Asn266Ser	CA126223 NM_001204261.2:c.797A>G