Canonical Allele Identifier: PA100022
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13453
ClinVar RCV Id: RCV000014395 RCV000236623 RCV000763027 RCV002433455
ClinVar Variation Id: 845368
ClinVar RCV Id: RCV001048418 RCV001173295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Phe84Leu
CA256847
NM_000371.3:c.250T>C
CA402156987
NM_000371.3:c.252T>G
CA402156988
NM_000371.3:c.252T>A