Original source

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

Alleles
TCAA/-
Location

Chromosome 4:174491347-174491350 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140833916

This variation has 5 HGVS names - click the plus to show

Variation displays