Canonical Allele Identifier: PA093982
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 987298
ClinVar RCV Id: RCV001268624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Gly88Val
CA393032364
NM_014249.4:c.263G>T