Canonical Allele Identifier: PA2499282682
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065725
ClinVar RCV Id: RCV001376380 RCV001871986 RCV003462941 RCV003888075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Gly51Arg
CA7640229
NM_016346.4:c.151G>A
CA393031992
NM_016346.4:c.151G>C