NM_213599.3(ANO5):c.692G>T (p.Gly231Val) AND not provided
- Germline classification:
- Pathogenic (11 submissions)
- Last evaluated:
- Dec 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000082853.47
Allele description
NM_213599.3(ANO5):c.692G>T (p.Gly231Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: May 1, 2024