NM_181882.3(PRX):c.2645T>C (p.Val882Ala) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Mar 3, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001705851.3
Allele description [Variation Report for NM_181882.3(PRX):c.2645T>C (p.Val882Ala)]
NM_181882.3(PRX):c.2645T>C (p.Val882Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024