NM_002471.4(MYH6):c.1462C>G (p.Gln488Glu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002224400.1
Allele description [Variation Report for NM_002471.4(MYH6):c.1462C>G (p.Gln488Glu)]
NM_002471.4(MYH6):c.1462C>G (p.Gln488Glu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023