Original source

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

Alleles
-/T
Location

Chromosome 14: between 92096910 and 92096911 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71123315

This variation has 50 HGVS names - click the plus to show

Variation displays