NM_018055.5(NODAL):c.*722G>C AND Heterotaxy, visceral, 5, autosomal
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000366778.5
Allele description [Variation Report for NM_018055.5(NODAL):c.*722G>C]
NM_018055.5(NODAL):c.*722G>C
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023