Canonical Allele Identifier: PA100134
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13421
ClinVar RCV Id: RCV000014363 RCV000159427 RCV001173293 RCV000852477 RCV002453258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Thr80Ala
CA256798
NM_000371.3:c.238A>G