NM_005477.3(HCN4):c.2838C>T (p.Pro946=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 5, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000428272.1
Allele description
NM_005477.3(HCN4):c.2838C>T (p.Pro946=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Jun 15, 2021