Original source

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

Alleles
CATC/-
Location

Chromosome 1:173878819-173878822 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 364

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

1:g.173878819_173878822delCATC
ENST00000367698.3:c.1021_1024delGATG
ENSP00000356671.3:p.Asp341AsnfsTer5

Variation displays