NM_001083116.3(PRF1):c.1310C>T (p.Ala437Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002520610.2
Allele description [Variation Report for NM_001083116.3(PRF1):c.1310C>T (p.Ala437Val)]
NM_001083116.3(PRF1):c.1310C>T (p.Ala437Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
crustin 2 [Procambarus clarkii]
crustin 2 [Procambarus clarkii]gi|328899144|gb|AEB54630.1|Protein
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Last Updated: Oct 8, 2024