NM_000551.4(VHL):c.167C>G (p.Ala56Gly) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000530730.8
-
Homo sapiens formin 2 (FMN2), transcript variant 3, mRNA
Homo sapiens formin 2 (FMN2), transcript variant 3, mRNAgi|1675094460|ref|NM_001348094.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jun 17, 2024