NM_000552.5(VWF):c.3802C>A (p.His1268Asn) AND not provided
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000086677.1
Allele description [Variation Report for NM_000552.5(VWF):c.3802C>A (p.His1268Asn)]
NM_000552.5(VWF):c.3802C>A (p.His1268Asn)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022