Original source

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

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

Chromosome 12:52676315 (forward strand) | View in location tab


with HGMD-PUBLIC CM990774 ; PhenCode HIFD_KRT1:c.1435A>T (T/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

Variation displays