Allele Registry

Canonical Allele Identifier: PA256858

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014402

ClinVar Variation:

13460

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Val142del	CA256856 NM_000371.3:c.424_426del