Canonical Allele Identifier: PA099799
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13436
ClinVar RCV Id: RCV000014378
ClinVar Variation Id: 13459
ClinVar RCV Id: RCV000014401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Gly67Arg
CA256816
NM_000371.3:c.199G>C
CA256855
NM_000371.3:c.199G>A