Canonical Allele Identifier: PA2573168647
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1490986
ClinVar RCV Id: RCV001986200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Cys30Tyr
CA402156507
NM_000371.3:c.89G>A