NM_021954.4(GJA3):c.715G>C (p.Gly239Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003248948.2
Allele description [Variation Report for NM_021954.4(GJA3):c.715G>C (p.Gly239Arg)]
NM_021954.4(GJA3):c.715G>C (p.Gly239Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
argonaute 2, isoform E [Drosophila melanogaster]
argonaute 2, isoform E [Drosophila melanogaster]gi|442632519|ref|NP_001261882.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024