NM_006214.4(PHYH):c.792C>T (p.His264=) AND PHYH-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003977863.1
Allele description [Variation Report for NM_006214.4(PHYH):c.792C>T (p.His264=)]
NM_006214.4(PHYH):c.792C>T (p.His264=)
Condition(s)
- Name:
- PHYH-related disorder
- Synonyms:
- PHYH-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024