NM_001103.4(ACTN2):c.1901C>T (p.Ala634Val) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003806089.1
Allele description [Variation Report for NM_001103.4(ACTN2):c.1901C>T (p.Ala634Val)]
NM_001103.4(ACTN2):c.1901C>T (p.Ala634Val)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024