NM_006063.3(KLHL41):c.1186G>T (p.Val396Leu) AND Nemaline myopathy 9
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000652022.9
Allele description [Variation Report for NM_006063.3(KLHL41):c.1186G>T (p.Val396Leu)]
NM_006063.3(KLHL41):c.1186G>T (p.Val396Leu)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024