Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
CT/-
Location

Chromosome 1:173909737-173909738 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 363

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

1:g.173909737_173909738delCT
ENST00000487183.1:n.618_619delAG
ENST00000367698.3:c.967_968delAG
ENSP00000356671.3:p.Ser323ProfsTer19
ENST00000617423.2:c.559+2126_559+2127delAG

Variation displays