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 () at this location.
Chromosome 12: between 33016384 and 33016385 (forward strand) | View in location tab
Archive dbSNP rs17064629
This variation has 5 HGVS names - click the plus to show