NM_031935.3(HMCN1):c.4857T>C (p.His1619=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002059370.6
Allele description [Variation Report for NM_031935.3(HMCN1):c.4857T>C (p.His1619=)]
NM_031935.3(HMCN1):c.4857T>C (p.His1619=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024