Allele Registry

Canonical Allele Identifier: PA100111

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014383

ClinVar Variation:

13441

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Thr69Ala	CA256827 NM_000371.3:c.205A>G