NM_001008216.2(GALE):c.912G>A (p.Val304=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Apr 27, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000242891.11
Allele description [Variation Report for NM_001008216.2(GALE):c.912G>A (p.Val304=)]
NM_001008216.2(GALE):c.912G>A (p.Val304=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024