NM_001103.4(ACTN2):c.1757T>C (p.Ile586Thr) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003803978.1
Allele description
NM_001103.4(ACTN2):c.1757T>C (p.Ile586Thr)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024