Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 12:52676318 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023635 ; PhenCode HIFD_KRT1:c.1432G>A (C/T), HIFD_KRT1:c.1432G>C (C/G)

Most severe consequence
Clinical significance

Synonyms

LSDB KRT1:c.1432G>C, KRT1:c.1432G>A

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

Variation displays