Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/TGC/GCT
Location

Chromosome 17: between 26724874 and 26724875 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146452556

This variation has 20 HGVS names - click the plus to show

Variation displays