NM_001042545.2(LTBP4):c.658G>T (p.Gly220Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003211328.2
Allele description [Variation Report for NM_001042545.2(LTBP4):c.658G>T (p.Gly220Cys)]
NM_001042545.2(LTBP4):c.658G>T (p.Gly220Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Drosophila melanogaster Neprilysin-like 20 (Nepl20), mRNA
Drosophila melanogaster Neprilysin-like 20 (Nepl20), mRNAgi|442621589|ref|NM_143388.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024