Original source

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

Alleles
AGCT/-
Location

Chromosome 2:127423120-127423123 (forward strand) | View in location tab

Most severe consequence
Synonyms

LSDB PC-HY10

This variation has 11 HGVS names - click the plus to show

Variation displays