Allele Registry

Canonical Allele Identifier: PA100165

Gene: TTR HGNC NCBI

ClinVar Allele:

28488

ClinVar RCV:

RCV000014391

ClinVar Variation:

13449

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Tyr134His	CA123104 NM_000371.3:c.400T>C