Original source

Variation features from SGRP, with Ensembl identifiers | About SGRP

Alleles
A/G | Ambiguity code: R
Location

Chromosome II:316976 (forward strand) | View in location tab

Most severe consequence

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2 individual genotypes.

Variation displays