NM_005557.4(KRT16):c.17G>T (p.Arg6Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003173503.2
Allele description [Variation Report for NM_005557.4(KRT16):c.17G>T (p.Arg6Leu)]
NM_005557.4(KRT16):c.17G>T (p.Arg6Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Rattus norvegicus hyaluronan and proteoglycan link protein 1 (Hapln1), mRNA
Rattus norvegicus hyaluronan and proteoglycan link protein 1 (Hapln1), mRNAgi|9506518|ref|NM_019189.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024