Allele Registry

Canonical Allele Identifier: PA100134

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014363

RCV000159427

RCV000852477

RCV001173293

RCV002453258

ClinVar Variation:

13421

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Thr80Ala	CA256798 NM_000371.3:c.238A>G