Canonical Allele Identifier: PA891846324
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 565560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Ala39Asp
CA402156622
NM_000371.3:c.116C>A