Allele Registry

Canonical Allele Identifier: PA658801691

Gene: TTR HGNC NCBI

ClinVar Allele:

532250

ClinVar RCV:

RCV000647353

ClinVar Variation:

538164

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Thr69Ser	CA402156902 NM_000371.3:c.205A>T CA402156905 NM_000371.3:c.206C>G