NM_001330585.2(CC2D1B):c.2254T>G (p.Phe752Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004270353.1
Allele description [Variation Report for NM_001330585.2(CC2D1B):c.2254T>G (p.Phe752Val)]
NM_001330585.2(CC2D1B):c.2254T>G (p.Phe752Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens cDNA FLJ52306 complete cds, highly similar to Kelch-like protein 1
Homo sapiens cDNA FLJ52306 complete cds, highly similar to Kelch-like protein 1gi|221041093|dbj|AK295939.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024