Allele Registry

Canonical Allele Identifier: PA297528

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000159430

RCV000246043

RCV000474573

RCV000769524

RCV000996672

RCV001173539

RCV004551363

ClinVar Variation:

181697

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Arg5His	CA297526 NM_000371.3:c.14G>A