Canonical Allele Identifier: PA2828132061
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16149
ClinVar RCV Id: RCV000017531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351110.1:p.Leu753Phe
CA126221
NM_001364181.2:c.2259A>T
CA361868551
NM_001364181.2:c.2259A>C