Canonical Allele Identifier: PA253523
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 5533
ClinVar Variation Id: 1076269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Gly56Arg
CA253522
NM_016346.4:c.166G>A
CA393032028
NM_016346.4:c.166G>C