NM_001106.4(ACVR2B):c.771C>T (p.Leu257=) AND Heterotaxy, visceral, 4, autosomal
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001511861.5
Allele description [Variation Report for NM_001106.4(ACVR2B):c.771C>T (p.Leu257=)]
NM_001106.4(ACVR2B):c.771C>T (p.Leu257=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024