NM_006269.2(RP1):c.2615G>A (p.Arg872His) AND Retinitis pigmentosa
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000277987.13
Allele description [Variation Report for NM_006269.2(RP1):c.2615G>A (p.Arg872His)]
NM_006269.2(RP1):c.2615G>A (p.Arg872His)
Condition(s)
-
we19g01.x1 NCI_CGAP_Lu24 Homo sapiens cDNA clone IMAGE:2341584 3', mRNA sequence
we19g01.x1 NCI_CGAP_Lu24 Homo sapiens cDNA clone IMAGE:2341584 3', mRNA sequencegi|4985901|gnl|dbEST|2602539|gb|AI6 .1|Nucleotide
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Last Updated: Oct 8, 2024