Canonical Allele Identifier: PA179469
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13458
ClinVar RCV Id: RCV000014400 RCV000152543 RCV000621591 RCV000586735 RCV001173296 RCV001170383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Arg124His
CA179467
NM_000371.3:c.371G>A