Canonical Allele Identifier: PA100258
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13440
ClinVar RCV Id: RCV000014382 RCV001173291 RCV002390107
ClinVar Variation Id: 2138144
ClinVar RCV Id: RCV003050501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Val50Leu
CA256825
NM_000371.3:c.148G>C
CA402156746
NM_000371.3:c.148G>T