Canonical Allele Identifier: PA2741957399
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2971863
ClinVar RCV Id: RCV003832925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Asn65Lys
CA393032093
NM_016346.4:c.195C>A
CA393032094
NM_016346.4:c.195C>G