NM_000132.4(F8):c.5587-98G>A AND Abnormality of coagulation
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000851821.1
Allele description [Variation Report for NM_000132.4(F8):c.5587-98G>A]
NM_000132.4(F8):c.5587-98G>A
Condition(s)
- Name:
- Abnormality of coagulation
- Identifiers:
- MedGen: C1846821; Human Phenotype Ontology: HP:0001928
-
Homo sapiens purinergic receptor P2X 2 (P2RX2), transcript variant 4, mRNA
Homo sapiens purinergic receptor P2X 2 (P2RX2), transcript variant 4, mRNAgi|531990822|ref|NM_170683.3|Nucleotide
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Last Updated: Apr 23, 2022