NM_002156.5(HSPD1):c.1446T>C (p.Asn482=) AND Hereditary spastic paraplegia 13
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000395839.5
Allele description [Variation Report for NM_002156.5(HSPD1):c.1446T>C (p.Asn482=)]
NM_002156.5(HSPD1):c.1446T>C (p.Asn482=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024