Canonical Allele Identifier: PA270111
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 143147

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Arg122Cys
CA270110
NM_014249.4:c.364C>T