NM_000313.4(PROS1):c.909G>A (p.Ala303=) AND Thrombophilia due to protein S deficiency, autosomal recessive
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001917016.5
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Homo sapiens heterogeneous nuclear ribonucleoprotein A0 (HNRNPA0), mRNA
Homo sapiens heterogeneous nuclear ribonucleoprotein A0 (HNRNPA0), mRNAgi|52426775|ref|NM_006805.3|Nucleotide
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LOC130005018 [Homo sapiens]
LOC130005018 [Homo sapiens]Gene ID:130005018Gene
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LOC130004917 [Homo sapiens]
LOC130004917 [Homo sapiens]Gene ID:130004917Gene
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LOC126861090 [Homo sapiens]
LOC126861090 [Homo sapiens]Gene ID:126861090Gene
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LOC130004897 [Homo sapiens]
LOC130004897 [Homo sapiens]Gene ID:130004897Gene
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024