NM_016011.5(MECR):c.830C>T (p.Ala277Val) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jun 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000962828.26
Allele description [Variation Report for NM_016011.5(MECR):c.830C>T (p.Ala277Val)]
NM_016011.5(MECR):c.830C>T (p.Ala277Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 15, 2024