NM_000439.5(PCSK1):c.1221G>A (p.Met407Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002743518.2
Allele description [Variation Report for NM_000439.5(PCSK1):c.1221G>A (p.Met407Ile)]
NM_000439.5(PCSK1):c.1221G>A (p.Met407Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024