NM_001106.4(ACVR2B):c.702C>T (p.Phe234=) AND Heterotaxy, visceral, 4, autosomal
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002899766.2
Allele description [Variation Report for NM_001106.4(ACVR2B):c.702C>T (p.Phe234=)]
NM_001106.4(ACVR2B):c.702C>T (p.Phe234=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024