Original source

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

Alleles
A/C/G | Ambiguity code: V
Location

This variation has not been mapped

Evidence status

This variation has 4 synonyms - click the plus to show

HGVS name

None

Variation displays