NM_001018115.3(FANCD2):c.983G>A (p.Arg328Gln) AND not provided
Clinical significance:Likely benign (Last evaluated: Oct 3, 2016)
Review status:
- Based on:
- 1 submission [Details]
- Record status:
- current
- Accession:
- RCV000443739.5
Allele description [Variation Report for NM_001018115.3(FANCD2):c.983G>A (p.Arg328Gln)]
NM_001018115.3(FANCD2):c.983G>A (p.Arg328Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jan 7, 2023