NM_000764.3(CYP2A7):c.1191C>T (p.Ser397=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 22, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000949842.3
Allele description
NM_000764.3(CYP2A7):c.1191C>T (p.Ser397=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Charcot-Marie-Tooth disease axonal type 2F
Charcot-Marie-Tooth disease axonal type 2FMedGen
-
C1847823[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023