This variation maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ambiguity code: Y
Location

This variation maps to 2 genomic locations; None selected

HGVS name

None

About this variant

This variant overlaps 1 transcript.

Variation displays