NM_002381.5(MATN3):c.636A>G (p.Ala212=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 13, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000924532.7
Allele description [Variation Report for NM_002381.5(MATN3):c.636A>G (p.Ala212=)]
NM_002381.5(MATN3):c.636A>G (p.Ala212=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024