NM_000525.3(KCNJ11):c.1009G>A (p.Val337Ile) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Feb 8, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000146099.2
Allele description
NM_000525.3(KCNJ11):c.1009G>A (p.Val337Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 23, 2021