Canonical Allele Identifier: PA2829751293
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 438228
ClinVar RCV Id: RCV000504861 RCV001003093 RCV001039719 RCV002226466 RCV003464083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Arg104Gln
CA7640282
NM_014249.4:c.311G>A