Source: NC_003283.11:g.10766577G>A
Genes: F28H7.12 (Cel), ocr-1 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:10766577G>A