Original source

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

Alleles
CT/-
Location

Chromosome 1:173878875-173878876 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 363

This variation has 4 HGVS names - click the plus to show

1:g.173878875_173878876delCT
ENST00000487183.1:n.618_619delAG
ENST00000367698.3:c.967_968delAG
ENSP00000356671.3:p.Ser323ProfsTer19

Variation displays