NM_000335.5(SCN5A):c.*1691G>T AND Congenital long QT syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000387525.5
Allele description [Variation Report for NM_000335.5(SCN5A):c.*1691G>T]
NM_000335.5(SCN5A):c.*1691G>T
Condition(s)
-
Conserved Domain Links for Gene (Select 400629) (1)
Conserved Domains
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 21, 2023