Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 5:254466 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs1804432

HGVS names

This variant has 19 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and 1 regulatory feature.

Variant displays