Canonical Allele Identifier: PA2829751090
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 843880
ClinVar RCV Id: RCV001046593 RCV001827289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Val49Leu
CA393031980
NM_014249.4:c.145G>C
CA393031981
NM_014249.4:c.145G>T