Allele Registry

Canonical Allele Identifier: PA101176

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017534

ClinVar Variation:

16152

HGVS (amino-acid)	Matching Registered Transcripts
NP_000167.1:p.Ile747Met	CA126227 NM_000176.3:c.2241T>G