NM_000552.5(VWF):c.4693G>T (p.Val1565Leu) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000244522.15
Allele description [Variation Report for NM_000552.5(VWF):c.4693G>T (p.Val1565Leu)]
NM_000552.5(VWF):c.4693G>T (p.Val1565Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
rhgA [Aspergillus niger]
rhgA [Aspergillus niger]Gene ID:4985445Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024