Original source

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

Alleles
TTTA/-
Location

Chromosome 5:135030021-135030024 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57888587

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

Variation displays