NM_006031.6(PCNT):c.8771G>A (p.Arg2924His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002556948.2
Allele description [Variation Report for NM_006031.6(PCNT):c.8771G>A (p.Arg2924His)]
NM_006031.6(PCNT):c.8771G>A (p.Arg2924His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024