Original source

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

Alleles
AC/-
Location

Chromosome 13:113301695-113301696 (forward strand) | View in location tab

Most severe consequence

This variation has 2 HGVS names - click the plus to show

Variation displays