Original source

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

Alleles
GA/-
Location

Chromosome 12:102147248-102147249 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_024312.4:c.3503_3504delTC

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

12:g.102147248_102147249delGA
ENST00000299314.7:c.3503_3504delTC
ENSP00000299314.7:p.Leu1168GlnfsTer5
ENST00000549738.1:c.*110_*111delTC

Variation displays