NM_174936.4(PCSK9):c.1851C>T (p.Ala617=) AND Familial hypercholesterolemia
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000771236.3
Allele description [Variation Report for NM_174936.4(PCSK9):c.1851C>T (p.Ala617=)]
NM_174936.4(PCSK9):c.1851C>T (p.Ala617=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024