NM_002292.4(LAMB2):c.938A>G (p.Lys313Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003164230.2
Allele description [Variation Report for NM_002292.4(LAMB2):c.938A>G (p.Lys313Arg)]
NM_002292.4(LAMB2):c.938A>G (p.Lys313Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
txid761763[Organism:noexp] (2)
Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024