NM_001909.5(CTSD):c.639C>G (p.Pro213=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Oct 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000675953.17
Allele description [Variation Report for NM_001909.5(CTSD):c.639C>G (p.Pro213=)]
NM_001909.5(CTSD):c.639C>G (p.Pro213=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024