Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 12:52886452 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM076258, CM990783 ; PhenCode HIFD_KRT6A:c.521T>C (A/G), HIFD_KRT6A:c.521T>G (A/C)

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Variation displays