NM_000528.4(MAN2B1):c.2670A>G (p.Ser890=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001702750.2
Allele description [Variation Report for NM_000528.4(MAN2B1):c.2670A>G (p.Ser890=)]
NM_000528.4(MAN2B1):c.2670A>G (p.Ser890=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024