Canonical Allele Identifier: PA2829751158
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2971863
ClinVar RCV Id: RCV003832925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Asn65Lys
CA393032093
NM_014249.4:c.195C>A
CA393032094
NM_014249.4:c.195C>G