NM_000217.3(KCNA1):c.53A>C (p.His18Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003168608.3
Allele description [Variation Report for NM_000217.3(KCNA1):c.53A>C (p.His18Pro)]
NM_000217.3(KCNA1):c.53A>C (p.His18Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Phodopus roborovskii voucher IPEE RAS:2739 cytochrome b gene, complete cds; mito...
Phodopus roborovskii voucher IPEE RAS:2739 cytochrome b gene, complete cds; mitochondrialgi|410609058|gb|JQ771086.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 12, 2024