Allele Registry

Canonical Allele Identifier: PA099889

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014388

RCV001288934

RCV002426503

RCV002476966

ClinVar Variation:

13446

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ile88Leu	CA256837 NM_000371.3:c.262A>T CA402157008 NM_000371.3:c.262A>C