NM_170665.4(ATP2A2):c.1983C>T (p.Asn661=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003258755.2
Allele description [Variation Report for NM_170665.4(ATP2A2):c.1983C>T (p.Asn661=)]
NM_170665.4(ATP2A2):c.1983C>T (p.Asn661=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Rattus norvegicus matrix metallopeptidase 12 (Mmp12), mRNA
Rattus norvegicus matrix metallopeptidase 12 (Mmp12), mRNAgi|291327536|ref|NM_053963.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024