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

This variation has 5 synonyms - click the plus to show

HGVS name

None

Variation displays