Allele Registry

Canonical Allele Identifier: PA100071

Gene: TTR HGNC NCBI

ClinVar Allele:

28478

ClinVar RCV:

RCV000014381

ClinVar Variation:

13439

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ser70Ile	CA256823 NM_000371.3:c.209G>T