Original source

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

Alleles
A/T/C | Ambiguity code: H
Location

This variation has not been mapped

Synonyms

LSDB NG_029922.1:g.9496C>T, NG_029922.1:g.9496C>A

HGVS name

None

Variation displays