Original source

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

Alleles
-/T
Location

Chromosome 2: between 96930970 and 96930971 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_017849.3:c.149_150insA

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

2:g.96930970_96930971insT
ENST00000258439.3:c.149dupA
ENSP00000258439.2:p.Pro51AlafsTer57
ENST00000432959.1:c.149dupA
ENSP00000416660.1:p.Pro51AlafsTer57

Variation displays