Original source

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

Alleles
-/T/TTA
Location

Chromosome 20: between 58671425 and 58671426 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 32 HGVS names - click the plus to show

Variation displays