NM_000500.9(CYP21A2):c.1430T>C (p.Phe477Ser) AND CYP21A2-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 18, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003951808.1
Allele description [Variation Report for NM_000500.9(CYP21A2):c.1430T>C (p.Phe477Ser)]
NM_000500.9(CYP21A2):c.1430T>C (p.Phe477Ser)
Condition(s)
- Name:
- CYP21A2-related disorder
- Synonyms:
- CYP21A2-related condition
- Identifiers:
-
Homo sapiens transmembrane protein 63C, mRNA (cDNA clone MGC:168227 IMAGE:902060...
Homo sapiens transmembrane protein 63C, mRNA (cDNA clone MGC:168227 IMAGE:9020604), complete cdsgi|187953290|gb|BC136614.1|Nucleotide
-
protein NETWORKED 1D-like [Cucurbita maxima]
protein NETWORKED 1D-like [Cucurbita maxima]gi|1281015671|ref|XP_022991964.1|Protein
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Last Updated: May 26, 2024