This variation has been flagged

Variation maps to 2 genomic locations

Select a location:
Original source

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

Alleles
G/A | Ambiguity code: R
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

Uniprot VAR_011323

HGVS name

None

Variation displays