NM_194318.4(B3GLCT):c.621A>T (p.Glu207Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002818713.2
Allele description [Variation Report for NM_194318.4(B3GLCT):c.621A>T (p.Glu207Asp)]
NM_194318.4(B3GLCT):c.621A>T (p.Glu207Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
zinc finger RNA-binding protein isoform 1 [Mus musculus]
zinc finger RNA-binding protein isoform 1 [Mus musculus]gi|168480106|ref|NP_035897.2|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024