Allele Registry

Canonical Allele Identifier: PA123111

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014396

RCV000714133

RCV001056317

RCV001173297

RCV002354162

ClinVar Variation:

13454

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ala129Val	CA123109 NM_000371.3:c.386C>T