NM_007184.4(NISCH):c.2789G>A (p.Arg930His) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- May 17, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000949693.4
Allele description [Variation Report for NM_007184.4(NISCH):c.2789G>A (p.Arg930His)]
NM_007184.4(NISCH):c.2789G>A (p.Arg930His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024