NM_000129.4(F13A1):c.1777G>A (p.Gly593Ser) 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:
- RCV000998514.9
Allele description [Variation Report for NM_000129.4(F13A1):c.1777G>A (p.Gly593Ser)]
NM_000129.4(F13A1):c.1777G>A (p.Gly593Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 4, 2024