NM_000173.7(GP1BA):c.137C>T (p.Pro46Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004047247.1
Allele description [Variation Report for NM_000173.7(GP1BA):c.137C>T (p.Pro46Leu)]
NM_000173.7(GP1BA):c.137C>T (p.Pro46Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
AL793549 XGC-neurula Xenopus tropicalis cDNA clone TNeu111e09 5', mRNA sequence
AL793549 XGC-neurula Xenopus tropicalis cDNA clone TNeu111e09 5', mRNA sequencegi|38315503|gnl|dbEST|20373423|emb| 549.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jun 23, 2024