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
G/A | Ancestral: G | Ambiguity code: R
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.PRO369LEU, 33004

HGVS name

None

Variation displays