Canonical Allele Identifier: PA099923
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Leu32Pro
CA256853
NM_000371.3:c.95T>C