Canonical Allele Identifier: PA100272
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13417
ClinVar RCV Id: RCV000014359 RCV000159423 RCV000770555 RCV001173292 RCV002390106 RCV002476964 RCV004549361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Val50Met
CA256790
NM_000371.3:c.148G>A