Allele Registry

Canonical Allele Identifier: PA916044697

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017534

ClinVar Variation:

16152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351114.1:p.Ile748Met	CA126227 NM_001364185.1:c.2244T>G