Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000260.4(MYO7A):c.1997G>A (p.Arg666Gln) | Uncertain Significance | Usher syndrome | 2020-05-20 | 1.0 | - | MYO7A |
Showing 1 to 1 of 1 rows