NM_000238.4(KCNH2):c.1864C>T (p.Leu622Phe) 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:
- RCV000058019.4
Allele description [Variation Report for NM_000238.4(KCNH2):c.1864C>T (p.Leu622Phe)]
NM_000238.4(KCNH2):c.1864C>T (p.Leu622Phe)
Condition(s)
-
mitochondrial basic amino acids transporter isoform X1 [Onychostruthus taczanows...
mitochondrial basic amino acids transporter isoform X1 [Onychostruthus taczanowskii]gi|2032632429|ref|XP_041254455.1|Protein
-
P2Y purinoceptor 1 [Meriones unguiculatus]
P2Y purinoceptor 1 [Meriones unguiculatus]gi|1211470800|ref|XP_021519703.1|Protein
-
S41 family peptidase [Spirosoma oryzicola]
S41 family peptidase [Spirosoma oryzicola]gi|2168319612|gnl|PRJNA784328|LQ777 5|gb|UHG92691.1|Protein
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Last Updated: Sep 29, 2024