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 () at this location.
Chromosome 12: between 32863450 and 32863451 (forward strand) | View in location tab
Archive dbSNP rs17064629
This variation has 10 HGVS names - click the plus to show