Allele Registry

Canonical Allele Identifier: PA101158

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017540

ClinVar Variation:

16157

HGVS (amino-acid)	Matching Registered Transcripts
NP_000167.1:p.Gly679Ser	CA126238 NM_000176.3:c.2035G>A