NM_016190.3(CRNN):c.77C>G (p.Thr26Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003387651.1
Allele description [Variation Report for NM_016190.3(CRNN):c.77C>G (p.Thr26Arg)]
NM_016190.3(CRNN):c.77C>G (p.Thr26Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
CRNN cornulin [Homo sapiens]
CRNN cornulin [Homo sapiens]Gene ID:49860Gene
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See more...Assertion and evidence details
Last Updated: Nov 4, 2023