NM_001393381.1(CRACD):c.2461G>C (p.Asp821His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004314591.1
Allele description [Variation Report for NM_001393381.1(CRACD):c.2461G>C (p.Asp821His)]
NM_001393381.1(CRACD):c.2461G>C (p.Asp821His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
R-spondin-1 isoform 1 precursor [Homo sapiens]
R-spondin-1 isoform 1 precursor [Homo sapiens]gi|84490388|ref|NP_001033722.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024