Canonical Allele Identifier: PA645455701
Gene: ROGDI HGNC NCBI

Linked Data

ClinVar Variation Id: 319401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078865.1:p.Leu209Val
CA7882611
NM_024589.3:c.625C>G