Canonical Allele Identifier: PA235939
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 191062
ClinVar RCV Id: RCV000171239 RCV001029779 RCV003989478
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Arg309Leu
CA235938
NM_014249.4:c.926G>T