Allele Registry

Canonical Allele Identifier: PA2826268926

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017529

ClinVar Variation:

16147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191187.1:p.Asp615Val	CA126218 NM_001204258.1:c.1844A>T