NM_000169.3(GLA):c.416A>G (p.Asn139Ser) AND not provided
- Germline classification:
- Likely benign (4 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001530102.7
Allele description [Variation Report for NM_000169.3(GLA):c.416A>G (p.Asn139Ser)]
NM_000169.3(GLA):c.416A>G (p.Asn139Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024