Canonical Allele Identifier: PA2573248103
Gene: NR4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1683962
ClinVar RCV Id: RCV002244484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006177.1:p.Ala53Val
CA348683058
NM_006186.4:c.158C>T