Canonical Allele Identifier: PA658811881
Gene: ROGDI HGNC NCBI

Linked Data

ClinVar Variation Id: 530799
ClinVar RCV Id: RCV000636836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078865.1:p.Arg130Trp
CA7882760
NM_024589.3:c.388C>T