Allele Registry

Canonical Allele Identifier: PA2826268920

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017535

ClinVar Variation:

16153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191187.1:p.Val545Ala	CA126229 NM_001204258.1:c.1634T>C