NM_005477.3(HCN4):c.2916C>T (p.Pro972=) AND HCN4-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 6, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004533277.1
Allele description [Variation Report for NM_005477.3(HCN4):c.2916C>T (p.Pro972=)]
NM_005477.3(HCN4):c.2916C>T (p.Pro972=)
Condition(s)
- Name:
- HCN4-related disorder
- Synonyms:
- HCN4-related condition
- Identifiers:
-
Homo sapiens V-set and transmembrane domain containing 2A (VSTM2A), transcript v...
Homo sapiens V-set and transmembrane domain containing 2A (VSTM2A), transcript variant 2, mRNAgi|1844283106|ref|NM_001301009.2|Nucleotide
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Last Updated: Sep 29, 2024