Allele Registry

Canonical Allele Identifier: PA2826269093

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017529

ClinVar Variation:

16147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191189.1:p.Asp552Val	CA126218 NM_001204260.2:c.1655A>T