NM_174936.4(PCSK9):c.1760A>G (p.Gln587Arg) AND Hypercholesterolemia, autosomal dominant, 3
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004007813.2
Allele description [Variation Report for NM_174936.4(PCSK9):c.1760A>G (p.Gln587Arg)]
NM_174936.4(PCSK9):c.1760A>G (p.Gln587Arg)
Condition(s)
-
wn89a04.x1 NCI_CGAP_Ut1 Homo sapiens cDNA clone IMAGE:2452974 3', mRNA sequence
wn89a04.x1 NCI_CGAP_Ut1 Homo sapiens cDNA clone IMAGE:2452974 3', mRNA sequencegi|5658137|gnl|dbEST|3044147|gb|AI9 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024