This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence (AA) at this location.
Chromosome 11:71441066-71441067 (forward strand) | View in location tab
This variation has 12 HGVS names - click the plus to show