NM_002474.3(MYH11):c.4016G>A (p.Arg1339His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000182515.3
Allele description [Variation Report for NM_002474.3(MYH11):c.4016G>A (p.Arg1339His)]
NM_002474.3(MYH11):c.4016G>A (p.Arg1339His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024