NM_001267550.2(TTN):c.104912C>T (p.Ala34971Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 3, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000734112.4
Allele description [Variation Report for NM_001267550.2(TTN):c.104912C>T (p.Ala34971Val)]
NM_001267550.2(TTN):c.104912C>T (p.Ala34971Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 29, 2024