Canonical Allele Identifier: PA297528
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 181697
ClinVar RCV Id: RCV000159430 RCV000246043 RCV000474573 RCV000769524 RCV000996672 RCV001173539 RCV004551363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Arg5His
CA297526
NM_000371.3:c.14G>A