NM_004333.6(BRAF):c.977T>C (p.Ile326Thr) AND Noonan syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001261042.2
Allele description [Variation Report for NM_004333.6(BRAF):c.977T>C (p.Ile326Thr)]
NM_004333.6(BRAF):c.977T>C (p.Ile326Thr)
Condition(s)
Assertion and evidence details
Last Updated: Jun 23, 2024