NM_000257.4(MYH7):c.4775G>A (p.Arg1592Gln) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001701153.4
Allele description [Variation Report for NM_000257.4(MYH7):c.4775G>A (p.Arg1592Gln)]
NM_000257.4(MYH7):c.4775G>A (p.Arg1592Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 3, 2024