Original source

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

Alleles
A/T/C/G | Ambiguity code: N
Location

This variation has not been mapped

Evidence status

Synonyms

LSDB NG_029922.1:g.9494G>T

HGVS name

None

Variation displays