NM_004448.4(ERBB2):c.2541C>T (p.Ala847=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001499764.9
Allele description [Variation Report for NM_004448.4(ERBB2):c.2541C>T (p.Ala847=)]
NM_004448.4(ERBB2):c.2541C>T (p.Ala847=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024