NM_001606.5(ABCA2):c.5972G>A (p.Arg1991His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 27, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004386978.1
Allele description [Variation Report for NM_001606.5(ABCA2):c.5972G>A (p.Arg1991His)]
NM_001606.5(ABCA2):c.5972G>A (p.Arg1991His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Homo sapiens semenogelin II mRNA, complete cds
Homo sapiens semenogelin II mRNA, complete cdsgi|338238|gb|M81652.1|HUMSMNGLNNucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024