NM_018192.4(P3H2):c.981G>A (p.Glu327=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001451436.5
Allele description [Variation Report for NM_018192.4(P3H2):c.981G>A (p.Glu327=)]
NM_018192.4(P3H2):c.981G>A (p.Glu327=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024