Original source

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

Alleles
TTTAT/-
Location

Chromosome 11:120262988-120262992 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144192477

This variation has 6 HGVS names - click the plus to show

Variation displays