Original source

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

Alleles
A/C|Ambiguity code: M
Location

Ultracontig Ultra103:375699 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Synonyms

Ensembl ENSOANSNP1147557

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript.

Variant displays