Canonical Allele Identifier: PA297550
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 181705
ClinVar RCV Id: RCV000159440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Ser18Ala
CA297548
NM_000371.3:c.52T>G