Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
TC/-
Location

Chromosome 12:43757176-43757177 (forward strand) | View in location tab

Most severe consequence

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts.

Variation displays