Canonical Allele Identifier: PA123103
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13434
ClinVar RCV Id: RCV000014376 RCV000036376 RCV000714134 RCV000618448 RCV000990084 RCV001170385 RCV001173303 RCV003993656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Thr139Met
CA123101
NM_000371.3:c.416C>T