Original source

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

Alleles
TC/-
Location

Chromosome 15:82823348-82823349 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB NM_001021.3:c.200_201delGA

This variation has 13 HGVS names - click the plus to show

Variation displays