NM_005236.3(ERCC4):c.2624A>G (p.Glu875Gly) AND not specified
Clinical significance:Benign
Review status:
- Based on:
- 4 submissions [Details]
- Record status:
- current
- Accession:
- RCV000116989.11
Allele description [Variation Report for NM_005236.3(ERCC4):c.2624A>G (p.Glu875Gly)]
NM_005236.3(ERCC4):c.2624A>G (p.Glu875Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 9, 2023
SCV000084972