Canonical Allele Identifier: PA100191
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1294424
ClinVar RCV Id: RCV001718568 RCV002440842 RCV003329411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Tyr98Phe
CA297739131
NM_000371.3:c.293A>T