NM_002291.3(LAMB1):c.2009T>C (p.Val670Ala) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 17, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000438823.1
Allele description [Variation Report for NM_002291.3(LAMB1):c.2009T>C (p.Val670Ala)]
NM_002291.3(LAMB1):c.2009T>C (p.Val670Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024