NM_001134707.2(SARDH):c.747G>A (p.Val249=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 30, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000947214.3
Allele description [Variation Report for NM_001134707.2(SARDH):c.747G>A (p.Val249=)]
NM_001134707.2(SARDH):c.747G>A (p.Val249=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023