Canonical Allele Identifier: PA182027
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 178280
ClinVar RCV Id: RCV000155021 RCV000766993 RCV000474349 RCV001173294 RCV001798511 RCV002408691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Phe64Leu
CA182025
NM_000371.3:c.190T>C
CA402156869
NM_000371.3:c.192T>A
CA402156870
NM_000371.3:c.192T>G