Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M
Location

Chromosome 14:28768627 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and 1 regulatory feature.

Variant displays