NM_000238.4(KCNH2):c.2902C>G (p.Pro968Ala) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 24, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000712076.10
Allele description [Variation Report for NM_000238.4(KCNH2):c.2902C>G (p.Pro968Ala)]
NM_000238.4(KCNH2):c.2902C>G (p.Pro968Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024