Allele Registry

Canonical Allele Identifier: PA099792

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014393

RCV000516227

RCV002415416

ClinVar Variation:

13451

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Gly67Ala	CA256845 NM_000371.3:c.200G>C