Canonical Allele Identifier: PA179463
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13427
ClinVar RCV Id: RCV000014369 RCV000152541 RCV000621211 RCV000770556 RCV000852746 RCV000857889 RCV001173306 RCV001256816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.His110Asn
CA179461
NM_000371.3:c.328C>A