NM_004285.4(H6PD):c.1053C>T (p.Gly351=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000974820.7
Allele description [Variation Report for NM_004285.4(H6PD):c.1053C>T (p.Gly351=)]
NM_004285.4(H6PD):c.1053C>T (p.Gly351=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024