This variation has been flagged

Variation maps to 3 genomic locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C/T | Ambiguity code: H
Location

This variation maps to 3 genomic locations; None selected

HGVS name

None

Variation displays