NM_018192.4(P3H2):c.266C>G (p.Ala89Gly) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001043009.4
Allele description [Variation Report for NM_018192.4(P3H2):c.266C>G (p.Ala89Gly)]
NM_018192.4(P3H2):c.266C>G (p.Ala89Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024