Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 12:53346565 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT18:c.1232G>A (G/A)

Most severe consequence
Evidence status

Synonyms

LSDB KRT18:c.1232G>A

This variation has 9 HGVS names - click the plus to show

Variation displays