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 (C) does not match the Ensembl reference sequence (CC) at this location.
Chromosome 1:115287840-115287841 (forward strand) | View in location tab
This variation has 8 HGVS names - click the plus to show