Canonical Allele Identifier: PA2829636386
Gene: NR4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 894762
ClinVar RCV Id: RCV001136357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006177.1:p.Gln109Lys
CA348682682
NM_006186.4:c.325C>A