Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
CTT/-
Location

Chromosome X:154765468-154765470 (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 15 HGVS names - click the plus to show

Variation displays