NM_174936.4(PCSK9):c.1323G>A (p.Val441=) AND Familial hypercholesterolemia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 22, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001523924.2
Allele description [Variation Report for NM_174936.4(PCSK9):c.1323G>A (p.Val441=)]
NM_174936.4(PCSK9):c.1323G>A (p.Val441=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 20, 2024