Original source

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

Alleles
ATA/-
Location

Chromosome 5:37001132-37001134 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 15883

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

5:g.37001132_37001134delATA
ENST00000448238.2:c.3616_3618delATA
ENSP00000406266.2:p.Ile1206del
ENST00000282516.8:c.3616_3618delATA
ENSP00000282516.8:p.Ile1206del

Variation displays