NM_006612.6(KIF1C):c.2318C>A (p.Ala773Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003282045.2
Allele description [Variation Report for NM_006612.6(KIF1C):c.2318C>A (p.Ala773Asp)]
NM_006612.6(KIF1C):c.2318C>A (p.Ala773Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus keratin 6B, mRNA (cDNA clone MGC:141272 IMAGE:40057433), complete c...
Mus musculus keratin 6B, mRNA (cDNA clone MGC:141272 IMAGE:40057433), complete cdsgi|110645787|gb|BC119555.1|Nucleotide
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Last Updated: May 1, 2024