Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 17:39665826 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_029445

HGVS names

This variant has 7 HGVS names - Show

About this variant

Variant displays