NM_000394.4(CRYAA):c.202C>T (p.Arg68Trp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 1, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000997832.18
Allele description
NM_000394.4(CRYAA):c.202C>T (p.Arg68Trp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
nuclear factor 1 A-type isoform 2 [Homo sapiens]
nuclear factor 1 A-type isoform 2 [Homo sapiens]gi|30840980|ref|NP_005586.1|Protein
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See more...Assertion and evidence details
Last Updated: Jun 17, 2024