NM_018341.3(ERMARD):c.9A>C (p.Val3=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 16, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000442041.1
Allele description [Variation Report for NM_018341.3(ERMARD):c.9A>C (p.Val3=)]
NM_018341.3(ERMARD):c.9A>C (p.Val3=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024