Allele Registry

Canonical Allele Identifier: PA099949

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014377

ClinVar Variation:

13435

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Leu78Arg	CA256814 NM_000371.3:c.233T>G