Original source

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

Alleles
A/C | Ambiguity code: M
Location

This variation has not been mapped

Evidence status

Synonyms

LSDB NG_029922.1:g.9498G>T

HGVS name

None

Variation displays