This variation has been flagged

Variation maps to 10 genomic locations

Select a location:
Original source

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

Alleles
A/G | Ambiguity code: R
Location

This variation maps to 10 genomic locations; None selected

Evidence status

Synonyms

Uniprot VAR_033394

HGVS name

None

Variation displays