Canonical Allele Identifier: PA2829751180
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 933381
ClinVar RCV Id: RCV001201582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Phe70Leu
CA393032120
NM_014249.4:c.208T>C
CA393032125
NM_014249.4:c.210C>A
CA393032126
NM_014249.4:c.210C>G