NM_022773.4(LMF1):c.1608G>T (p.Val536=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000908727.8
Allele description [Variation Report for NM_022773.4(LMF1):c.1608G>T (p.Val536=)]
NM_022773.4(LMF1):c.1608G>T (p.Val536=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024