Canonical Allele Identifier: PA2580220492
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2309408
ClinVar RCV Id: RCV002870492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351114.1:p.Val508Ala
CA3486847
NM_001364185.1:c.1523T>C