Allele Registry

Canonical Allele Identifier: PA891846322

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000703248

RCV002458294

ClinVar Variation:

579863

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ala12Ser	CA402156304 NM_000371.3:c.34G>T