Original source

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

Alleles
GA/-
Location

Chromosome 12:101753470-101753471 (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.101753470_101753471delGA
ENST00000299314.9:c.612delAinsCAGA
ENSP00000299314.7:p.Ser203dup
ENST00000549738.3:c.*110_*111delTC

Variation displays