This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP
Note: The reference base for this variant (CTAT) does not match the Ensembl reference base (T) at this location.
Chromosome 6:52341559 (forward strand) | View in location tab
This variation has 9 HGVS names - click the plus to show