NM_003977.4(AIP):c.591G>A (p.Glu197=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001065292.6
Allele description [Variation Report for NM_003977.4(AIP):c.591G>A (p.Glu197=)]
NM_003977.4(AIP):c.591G>A (p.Glu197=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024