NM_000439.5(PCSK1):c.282T>C (p.Asp94=) AND PCSK1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003896353.1
Allele description [Variation Report for NM_000439.5(PCSK1):c.282T>C (p.Asp94=)]
NM_000439.5(PCSK1):c.282T>C (p.Asp94=)
Condition(s)
- Name:
- PCSK1-related disorder
- Synonyms:
- PCSK1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Jun 2, 2024