Canonical Allele Identifier: PA126222
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16149
ClinVar RCV Id: RCV000017531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018087.1:p.Leu753Phe
CA126221
NM_001018077.1:c.2259A>T
CA361868551
NM_001018077.1:c.2259A>C