NM_000298.6(PKLR):c.1686C>T (p.Ser562=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000901437.23
Allele description [Variation Report for NM_000298.6(PKLR):c.1686C>T (p.Ser562=)]
NM_000298.6(PKLR):c.1686C>T (p.Ser562=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024