NM_001037132.4(NRCAM):c.2952G>C (p.Glu984Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 21, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004650421.1
Allele description [Variation Report for NM_001037132.4(NRCAM):c.2952G>C (p.Glu984Asp)]
NM_001037132.4(NRCAM):c.2952G>C (p.Glu984Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
AGENCOURT_6566935 NIH_MGC_88 Homo sapiens cDNA clone IMAGE:5736787 5', mRNA sequ...
AGENCOURT_6566935 NIH_MGC_88 Homo sapiens cDNA clone IMAGE:5736787 5', mRNA sequencegi|18809436|gnl|dbEST|11136326|gb|B 37.1|Nucleotide
-
tryptophan--tRNA ligase, cytoplasmic [Danio rerio]
tryptophan--tRNA ligase, cytoplasmic [Danio rerio]gi|41152126|ref|NP_957066.1|Protein
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Last Updated: Aug 11, 2024