This variation maps to 2 locations

Select a location:
Original source

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

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

This variation maps to 2 genomic locations; None selected

Synonyms

LSDB NG_029922.1:g.9496C>T, NG_029922.1:g.9496C>A

HGVS name

None

Variation displays