NM_174936.4(PCSK9):c.453C>T (p.Ala151=) AND Hypercholesterolemia, autosomal dominant, 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001473246.4
Allele description [Variation Report for NM_174936.4(PCSK9):c.453C>T (p.Ala151=)]
NM_174936.4(PCSK9):c.453C>T (p.Ala151=)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023