Canonical Allele Identifier: PA2741927485
Gene: NR4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2575592
ClinVar RCV Id: RCV003321158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006177.1:p.Gln5His
CA348683388
NM_006186.4:c.15G>T
CA348683389
NM_006186.4:c.15G>C