NM_002253.4(KDR):c.1055C>T (p.Ala352Val) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000865154.3
Allele description [Variation Report for NM_002253.4(KDR):c.1055C>T (p.Ala352Val)]
NM_002253.4(KDR):c.1055C>T (p.Ala352Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023