NM_000218.3(KCNQ1):c.875G>A (p.Gly292Asp) 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:
- RCV000057784.11
Allele description [Variation Report for NM_000218.3(KCNQ1):c.875G>A (p.Gly292Asp)]
NM_000218.3(KCNQ1):c.875G>A (p.Gly292Asp)
Condition(s)
-
IL3-CT0219-280100-062-G01 CT0219 Homo sapiens cDNA, mRNA sequence
IL3-CT0219-280100-062-G01 CT0219 Homo sapiens cDNA, mRNA sequencegi|7309056|gnl|dbEST|4037581|gb|AW6 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024