Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 13:113118491 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_013936

This variation has 7 HGVS names - click the plus to show

Variation displays