Canonical Allele Identifier: PA1139755941
Gene: ROGDI HGNC NCBI

Linked Data

ClinVar Variation Id: 860290
ClinVar RCV Id: RCV001066570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078865.1:p.Asp131Ala
CA394653336
NM_024589.3:c.392A>C