SCN7A

sodium voltage-gated channel alpha subunit 7
OMIM: 182392, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SCN7A in Fetal anomalies


Version 4.1
Latest signed off version: v4.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Holoprosencephaly