This variation maps to 2 locations

Select a location:
Original source

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

Alleles
TC/-
Location

This variation maps to 2 genomic locations; None selected

Clinical significance

Synonyms

LSDB NM_001021.3:c.200_201delGA

HGVS name

None

Variation displays