Canonical Allele Identifier: PA658811902
Gene: ROGDI HGNC NCBI

Linked Data

ClinVar Variation Id: 530794
ClinVar RCV Id: RCV000636831
ClinVar Variation Id: 659400
ClinVar RCV Id: RCV000816401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078865.1:p.Gly221Arg
CA7882562
NM_024589.3:c.661G>C
CA394649596
NM_024589.3:c.661G>A