Canonical Allele Identifier: PA2830326200
Gene: NR4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3064509
ClinVar RCV Id: RCV003989049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775265.1:p.Pro534Ser
CA348679236
NM_173173.3:c.1600C>T