NM_207034.3(EDN3):c.426G>A (p.Ala142=) AND Hirschsprung disease, susceptibility to, 4
- 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:
- RCV000339538.5
Allele description [Variation Report for NM_207034.3(EDN3):c.426G>A (p.Ala142=)]
NM_207034.3(EDN3):c.426G>A (p.Ala142=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024