Original source

Variants (including SNPs and indels) imported from dbSNP [remapped from build CAT] (release 127) | View in dbSNP

G/A | Ambiguity code: R

Chromosome A1:10132487 (forward strand) | View in location tab

Most severe consequence
Missense variant

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts.

Variant displays