NM_001110556.2(FLNA):c.2538C>T (p.Tyr846=) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 20, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000194585.13
Allele description [Variation Report for NM_001110556.2(FLNA):c.2538C>T (p.Tyr846=)]
NM_001110556.2(FLNA):c.2538C>T (p.Tyr846=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024