NM_001122659.3(EDNRB):c.561C>T (p.Ile187=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jan 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000969641.9
Allele description [Variation Report for NM_001122659.3(EDNRB):c.561C>T (p.Ile187=)]
NM_001122659.3(EDNRB):c.561C>T (p.Ile187=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024