Canonical Allele Identifier: PA093972
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 5533
ClinVar RCV Id: RCV000005871 RCV000286602 RCV000787628 RCV001075751
ClinVar Variation Id: 1076269
ClinVar RCV Id: RCV001390124 RCV003888089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Gly56Arg
CA253522
NM_014249.4:c.166G>A
CA393032028
NM_014249.4:c.166G>C