This variation maps to 3 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/G/T | Ambiguity code: B
Location

This variation maps to 3 genomic locations; None selected

Evidence status

This variation has 3 synonyms - click the plus to show

HGVS name

None

Variation displays