NM_020975.6(RET):c.2307G>T (p.Leu769=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Mar 23, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000153835.3
Allele description
NM_020975.6(RET):c.2307G>T (p.Leu769=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 15, 2021