NM_001039570.3(KREMEN1):c.141C>A (p.Asn47Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003367441.2
Allele description [Variation Report for NM_001039570.3(KREMEN1):c.141C>A (p.Asn47Lys)]
NM_001039570.3(KREMEN1):c.141C>A (p.Asn47Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens clk2 mRNA, complete cds
Homo sapiens clk2 mRNA, complete cdsgi|632967|gb|L29218.1|HUMCLK2BNucleotide
-
Nucleotide INSDC for Assembly (Select 10470891) (4021)
Nucleotide
-
Taxonomy Links for GEO Profiles (Select 85328155) (1)
Taxonomy
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024