NM_015340.4(LARS2):c.972C>A (p.His324Gln) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- May 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000220287.18
Allele description [Variation Report for NM_015340.4(LARS2):c.972C>A (p.His324Gln)]
NM_015340.4(LARS2):c.972C>A (p.His324Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024