Allele Registry

Canonical Allele Identifier: PA100092

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014364

RCV000519257

RCV001000742

RCV001173289

RCV002433454

RCV002504783

ClinVar Variation:

13422

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ser97Tyr	CA256800 NM_000371.3:c.290C>A