Canonical Allele Identifier: PA100212
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13426
ClinVar RCV Id: RCV000030575 RCV000014368 RCV000078674 RCV000211747 RCV000243161 RCV000735409 RCV000853387 RCV001173290 RCV003335038 RCV002476965 RCV003319166
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Val142Ile
CA214382
NM_000371.3:c.424G>A