Canonical Allele Identifier: PA100037
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 181693
ClinVar RCV Id: RCV000159421 RCV000560691 RCV002381523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Pro44Ser
CA297519
NM_000371.3:c.130C>T