NM_002474.3(MYH11):c.5454G>A (p.Ala1818=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 15, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001697957.9
Allele description [Variation Report for NM_002474.3(MYH11):c.5454G>A (p.Ala1818=)]
NM_002474.3(MYH11):c.5454G>A (p.Ala1818=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024