Canonical Allele Identifier: PA891846322
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 579863
ClinVar RCV Id: RCV000703248 RCV002458294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Ala12Ser
CA402156304
NM_000371.3:c.34G>T