NM_005477.3(HCN4):c.1459G>A (p.Val487Met) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001706022.10
Allele description [Variation Report for NM_005477.3(HCN4):c.1459G>A (p.Val487Met)]
NM_005477.3(HCN4):c.1459G>A (p.Val487Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024