Original source

Variants (including SNPs and indels) imported from dbSNP (release 143) | View in dbSNP

T/G | Ambiguity code: K

Chromosome 2:26997417 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 192 sample genotypes.

Variant displays