NM_172201.2(KCNE2):c.59T>A (p.Ile20Asn) AND Congenital long QT syndrome
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000058376.5
Allele description [Variation Report for NM_172201.2(KCNE2):c.59T>A (p.Ile20Asn)]
NM_172201.2(KCNE2):c.59T>A (p.Ile20Asn)
Condition(s)
-
BioSample links for Nucleotide (Select 2788978) (1)
BioSample
-
NCI_CGAP_GCB1
NCI_CGAP_GCB1biosample
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 14, 2023