Original source

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

Alleles
A/T/G | Ambiguity code: D
Location

This variation has not been mapped

Synonyms

LSDB NG_029922.1:g.9497T>G, NG_029922.1:g.9497T>A

HGVS name

None

Variation displays