Original source

Variation features from DPGP, with Ensembl identifiers (release 1) | DPGP 1

Alleles
G/A/C/T | Ambiguity code: N
Location

Chromosome 2L:1056714 (forward strand) | View in location tab

Most severe consequence

This variation has 9 HGVS names - click the plus to show

Variation displays