Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 9:711384 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_026212

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2 sample genotypes.

Variant displays