Canonical Allele Identifier: PA916077293
Gene: ROGDI HGNC NCBI

Linked Data

ClinVar Variation Id: 650621
ClinVar RCV Id: RCV000805803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078865.1:p.Arg218Cys
CA394649662
NM_024589.3:c.652C>T