Original source

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

Alleles
TAT/-
Location

Chromosome 17:65008808-65008810 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.65008808_65008810delTAT

Variation displays