NM_017534.6(MYH2):c.1491C>T (p.Phe497=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000977805.3
Allele description
NM_017534.6(MYH2):c.1491C>T (p.Phe497=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Mar 18, 2023