NM_000128.4(F11):c.467T>C (p.Phe156Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003212721.2
Allele description [Variation Report for NM_000128.4(F11):c.467T>C (p.Phe156Ser)]
NM_000128.4(F11):c.467T>C (p.Phe156Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Cnr2 protein [Mus musculus]
Cnr2 protein [Mus musculus]gi|23274013|gb|AAH24052.1|Protein
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Last Updated: May 1, 2024