NM_002474.3(MYH11):c.3291C>T (p.Ala1097=) AND MYH11-related condition
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003947544.1
Allele description [Variation Report for NM_002474.3(MYH11):c.3291C>T (p.Ala1097=)]
NM_002474.3(MYH11):c.3291C>T (p.Ala1097=)
Condition(s)
- Name:
- MYH11-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Mar 16, 2024