Original source

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

Alleles
-/CTT
Location

Chromosome 17: between 40819078 and 40819079 (forward strand) | View in location tab

Most severe consequence

This variation has 3 HGVS names - click the plus to show

Variation displays