Allele Registry

Canonical Allele Identifier: PA100037

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000159421

RCV000560691

RCV002381523

ClinVar Variation:

181693

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Pro44Ser	CA297519 NM_000371.3:c.130C>T