Source: NC_003281.10:g.1577382C>T
Genes: Y22D7AL.7 (Cel), Y22D7AL.t5 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:1577382C>T