Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
CTT/-
Location

Chromosome X:153993743-153993745 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_001363.3:c.109_111delCTT, 6819

This variation has 13 HGVS names - click the plus to show

Variation displays