NM_001377299.1(NDUFS2):c.660C>T (p.Ala220=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002927620.2
Allele description
NM_001377299.1(NDUFS2):c.660C>T (p.Ala220=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
AU140931 PLACE4 Homo sapiens cDNA clone PLACE4000517 5', mRNA sequence
AU140931 PLACE4 Homo sapiens cDNA clone PLACE4000517 5', mRNA sequencegi|11002452|gnl|dbEST|6569946|dbj|A 31.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 12, 2024