Allele Registry

Canonical Allele Identifier: PA099570

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014390

ClinVar Variation:

13448

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ala117Gly	CA256841 NM_000371.3:c.350C>G