NM_001267727.2(ARSG):c.1557C>T (p.Ala519=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 18, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001412957.14
Allele description
NM_001267727.2(ARSG):c.1557C>T (p.Ala519=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024