NM_153717.3(EVC):c.76G>T (p.Ala26Ser) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 27, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003065630.1
Allele description [Variation Report for NM_153717.3(EVC):c.76G>T (p.Ala26Ser)]
NM_153717.3(EVC):c.76G>T (p.Ala26Ser)
Condition(s)
Assertion and evidence details
Last Updated: Feb 13, 2023