NM_014874.4(MFN2):c.744C>T (p.Leu248=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003114277.3
Allele description [Variation Report for NM_014874.4(MFN2):c.744C>T (p.Leu248=)]
NM_014874.4(MFN2):c.744C>T (p.Leu248=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
disks large homolog 2 isoform 2 [Homo sapiens]
disks large homolog 2 isoform 2 [Homo sapiens]gi|91199538|ref|NP_001355.2|Protein
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Last Updated: May 7, 2024