NM_001112741.2(KCNC1):c.1204G>A (p.Gly402Ser) AND Inborn genetic diseases
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jul 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003356935.2
Allele description [Variation Report for NM_001112741.2(KCNC1):c.1204G>A (p.Gly402Ser)]
NM_001112741.2(KCNC1):c.1204G>A (p.Gly402Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Hepatitis B virus DNA, complete genome, strain: C0714154(WBK)F
Hepatitis B virus DNA, complete genome, strain: C0714154(WBK)Fgi|251822189|dbj|AP011098.1|Nucleotide
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Last Updated: May 1, 2024