Annotation Detail
Information
- Associated Genes
- TTR
- Associated Variants
-
TTR p.Leu32Pro (p.L32P)
(
ENST00000237014.8,
ENST00000610404.5,
ENST00000649620.1 )
TTR p.Leu32Pro (p.L32P) ( ENST00000237014.8, ENST00000610404.5, ENST00000649620.1 ) - Associated Disease
- Familial amyloid neuropathy
- Source Database
- ClinVar
- Description
- NM_000371.4(TTR):c.95T>C (p.Leu32Pro) AND Familial amyloid neuropathy
- ClinVar Allele ID
- 28496
- ClinVar RefSeq Alternation Syntax
- NM_000371.4:c.95T>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-06-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014399
- ClinVar Disease
- Familial amyloid neuropathy
- Observed Origin Sample
- germline
- Pubmed
- 10071047
Drugs