NM_002900.3(RBP3):c.1709C>T (p.Ala570Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002799093.2
Allele description [Variation Report for NM_002900.3(RBP3):c.1709C>T (p.Ala570Val)]
NM_002900.3(RBP3):c.1709C>T (p.Ala570Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
MCE family protein [Paracoccus liaowanqingii]
MCE family protein [Paracoccus liaowanqingii]gi|1608348849|gb|QBX34927.1||gnl|PR 9051|E4191_09535Protein
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See more...Assertion and evidence details
Last Updated: Jun 23, 2024