Original source

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

Alleles
AAA/-
Location

Chromosome 1:230711817-230711819 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs200548886, rs71876590

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

Variation displays