Canonical Allele Identifier: PA2830326081
Gene: NR4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2604027
ClinVar RCV Id: RCV003343150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775265.1:p.Met139Val
CA1916419
NM_173173.3:c.415A>G