NM_001206744.2(TPO):c.12C>G (p.Leu4=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001711550.3
Allele description [Variation Report for NM_001206744.2(TPO):c.12C>G (p.Leu4=)]
NM_001206744.2(TPO):c.12C>G (p.Leu4=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024