Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome X:18602444 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042956 ; PhenCode RettBASE_CDKL5:c.525A>T (A/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB CDKL5: c.525A>T, 6905

This variation has 5 HGVS names - click the plus to show

Variation displays