NM_001106.4(ACVR2B):c.993C>T (p.Ser331=) AND Heterotaxy, visceral, 4, autosomal
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000227436.11
Allele description [Variation Report for NM_001106.4(ACVR2B):c.993C>T (p.Ser331=)]
NM_001106.4(ACVR2B):c.993C>T (p.Ser331=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024