NM_000426.4(LAMA2):c.1814C>T (p.Thr605Ile) AND LAMA2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004532988.2
Allele description [Variation Report for NM_000426.4(LAMA2):c.1814C>T (p.Thr605Ile)]
NM_000426.4(LAMA2):c.1814C>T (p.Thr605Ile)
Condition(s)
- Name:
- LAMA2-related disorder
- Synonyms:
- LAMA2-related disorders; LAMA2-related condition
- Identifiers:
-
Homo sapiens IKK interacting protein, mRNA (cDNA clone IMAGE:3685751), partial c...
Homo sapiens IKK interacting protein, mRNA (cDNA clone IMAGE:3685751), partial cdsgi|77748092|gb|BC107572.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 26, 2024