NM_000014.6(A2M):c.53T>G (p.Leu18Arg) AND A2M-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 17, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003929799.2
Allele description [Variation Report for NM_000014.6(A2M):c.53T>G (p.Leu18Arg)]
NM_000014.6(A2M):c.53T>G (p.Leu18Arg)
Condition(s)
- Name:
- A2M-related disorder
- Synonyms:
- A2M-related condition
- Identifiers:
-
Mouse DNA sequence from clone RP23-461C4 on chromosome 11, complete sequence
Mouse DNA sequence from clone RP23-461C4 on chromosome 11, complete sequencegi|29603312|emb|AL954730.15|Nucleotide
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Last Updated: Oct 8, 2024