NM_022356.4(P3H1):c.1890T>C (p.Thr630=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000898956.3
Allele description
NM_022356.4(P3H1):c.1890T>C (p.Thr630=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022