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 (AG) at this location.
Chromosome X:120426651-120426652 (forward strand) | View in location tab
This variation has 6 HGVS names - click the plus to show