Gene HUMAN03972 (BWR1B_HUMAN)

E Homo sapiens | Beckwith-Wiedemann syndrome chromosomal region 1 c [SLC22A18AS]

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General Information

Descriptionsolute carrier family 22 member 18 antisense [Source:HGNC Symbol;Acc:HGNC:10965]; transcript_id=ENST00000526203.1
Organism HUMAN - Homo sapiens
Locus[ Chromosome 11 ]: 2888180 ... 2888632
Number of exons1
Exonscomplement(2888180..2888632)

IDs and Cross-references

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