Allele Registry

Canonical Allele Identifier: PA2825332446

Gene: NR3C1 HGNC NCBI

ClinVar Allele:

31191

ClinVar RCV:

RCV000017534

ClinVar Variation:

16152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019265.1:p.Ile748Met	CA126227 NM_001024094.2:c.2244T>G