Original source

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

Alleles
CCAGGGATGGTGGCA/-
Location

Chromosome 5:174725612-174725626 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs66988924

This variation has 3 HGVS names - click the plus to show

Variation displays