Allele Registry

Canonical Allele Identifier: PA099994

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014398

RCV001810860

RCV002390108

ClinVar Variation:

13456

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Phe53Leu	CA256851 NM_000371.3:c.157T>C CA402156787 NM_000371.3:c.159C>A CA402156789 NM_000371.3:c.159C>G