NM_000243.3(MEFV):c.1503C>T (p.Arg501=) AND not provided
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Oct 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001689576.18
Allele description [Variation Report for NM_000243.3(MEFV):c.1503C>T (p.Arg501=)]
NM_000243.3(MEFV):c.1503C>T (p.Arg501=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024