Original source

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

Alleles
-/TTAT
Location

Chromosome 18: between 77248354 and 77248355 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

18:g.77248354_77248355insTTAT

Variation displays