Canonical Allele Identifier: PA645506269
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 246201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Ile46Val
CA8928416
NM_000371.3:c.136A>G