NM_004673.4(ANGPTL1):c.976G>C (p.Asp326His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004241345.1
Allele description [Variation Report for NM_004673.4(ANGPTL1):c.976G>C (p.Asp326His)]
NM_004673.4(ANGPTL1):c.976G>C (p.Asp326His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Conserved Domain Links for Gene (Select 80712) (3)
Conserved Domains
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Last Updated: Jun 2, 2024