NM_002473.6(MYH9):c.4902C>T (p.Asp1634=) AND MYH9-related condition
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 4, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003938507.1
Allele description
NM_002473.6(MYH9):c.4902C>T (p.Asp1634=)
Condition(s)
- Name:
- MYH9-related condition
- Identifiers:
-
Legius Syndrome - GeneReviews®
Legius Syndrome - GeneReviews®
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Last Updated: Mar 16, 2024