Original source

Variants (including SNPs and indels) imported from dbSNP (release 139)|View in dbSNP

Alleles
G/C|Ambiguity code: S
Location

Chromosome 18:73163 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts.

Variant displays