NM_000238.4(KCNH2):c.1905C>G (p.Asn635Lys) 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:
- RCV000058047.5
Allele description [Variation Report for NM_000238.4(KCNH2):c.1905C>G (p.Asn635Lys)]
NM_000238.4(KCNH2):c.1905C>G (p.Asn635Lys)
Condition(s)
-
inpp4aa [Anoplopoma fimbria]
inpp4aa [Anoplopoma fimbria]Gene ID:129104462Gene
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See more...Assertion and evidence details
Last Updated: Nov 5, 2022