Canonical Allele Identifier: PA2829751248
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2146056
ClinVar RCV Id: RCV003066932 RCV003294437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Val85Leu
CA272574966
NM_014249.4:c.253G>T
CA393032323
NM_014249.4:c.253G>C