Canonical Allele Identifier: PA100144
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1075408
ClinVar RCV Id: RCV001389003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Trp61Leu
CA402156850
NM_000371.3:c.182G>T