Canonical Allele Identifier: PA100092
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13422
ClinVar RCV Id: RCV000014364 RCV000519257 RCV001000742 RCV001173289 RCV002504783 RCV002433454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Ser97Tyr
CA256800
NM_000371.3:c.290C>A