Allele Registry

Canonical Allele Identifier: PA100126

Gene: TTR HGNC NCBI

ClinVar Allele:

179807

ClinVar RCV:

RCV000159426

RCV003514316

ClinVar Variation:

181694

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Thr79Lys	CA297521 NM_000371.3:c.236C>A