This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (TC) at this location.
Chromosome 5:112153664-112153665 (forward strand) | View in location tab
This variation has 20 HGVS names - click the plus to show