Canonical Allele Identifier: PA1139762297
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_775265.1:p.Gln46Lys
CA348682682
NM_173173.3:c.136C>A