NM_000238.4(KCNH2):c.1825G>A (p.Asp609Asn) 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:
- RCV000058002.4
Allele description [Variation Report for NM_000238.4(KCNH2):c.1825G>A (p.Asp609Asn)]
NM_000238.4(KCNH2):c.1825G>A (p.Asp609Asn)
Condition(s)
-
Homo sapiens alkB homolog 8, tRNA methyltransferase (ALKBH8), transcript variant...
Homo sapiens alkB homolog 8, tRNA methyltransferase (ALKBH8), transcript variant 8, non-coding RNAgi|1802776481|ref|NR_165425.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024