Canonical Allele Identifier: PA2499231813
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1003248
ClinVar RCV Id: RCV001299780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Ala57Asp
CA402156823
NM_000371.3:c.170C>A