Allele Registry

Canonical Allele Identifier: PA2829751271

Gene: NR2E3 HGNC NCBI

ClinVar Variation Id: 867090

HGVS (amino-acid)	Matching Registered Transcripts
NP_055064.1:p.Arg97Cys	CA272574991 NM_014249.4:c.289C>T