NM_032578.4(MYPN):c.1884C>G (p.Phe628Leu) AND not provided
- Germline classification:
- Benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000024497.7
Allele description [Variation Report for NM_032578.4(MYPN):c.1884C>G (p.Phe628Leu)]
NM_032578.4(MYPN):c.1884C>G (p.Phe628Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024