NM_001348768.2(HECW2):c.1551A>C (p.Glu517Asp) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000892830.3
Allele description [Variation Report for NM_001348768.2(HECW2):c.1551A>C (p.Glu517Asp)]
NM_001348768.2(HECW2):c.1551A>C (p.Glu517Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022