Canonical Allele Identifier: PA891853168
Gene: ROGDI HGNC NCBI

Linked Data

ClinVar Variation Id: 582170
ClinVar RCV Id: RCV000706169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078865.1:p.Ala223Ser
CA7882559
NM_024589.3:c.667G>T