NM_003289.4(TPM2):c.813C>T (p.Ser271=) AND Congenital myopathy 23
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000325063.5
Allele description [Variation Report for NM_003289.4(TPM2):c.813C>T (p.Ser271=)]
NM_003289.4(TPM2):c.813C>T (p.Ser271=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024