Canonical Allele Identifier: PA297525
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 181695
ClinVar RCV Id: RCV000647355 RCV000725937 RCV001731489 RCV001173300 RCV002433710 RCV002478482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Asp94His
CA297523
NM_000371.3:c.280G>C