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

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript.

Variant displays