Canonical Allele Identifier: PA2826269020
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16158
ClinVar RCV Id: RCV000017541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191188.1:p.Phe652Leu
CA126240
NM_001204259.2:c.1954T>C
CA361868666
NM_001204259.2:c.1956C>G
CA361868667
NM_001204259.2:c.1956C>A