Original source

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

Alleles
G/C|Ambiguity code: S
Location

Chromosome 2L:145 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
HGVS name

2L:g.145G>C

About this variant

This variant has 1 sample genotype.

Variant displays