NM_000432.4(MYL2):c.496G>A (p.Asp166Asn) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001751627.2
Allele description [Variation Report for NM_000432.4(MYL2):c.496G>A (p.Asp166Asn)]
NM_000432.4(MYL2):c.496G>A (p.Asp166Asn)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024