Canonical Allele Identifier: PA099975
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 13443
ClinVar RCV Id: RCV000014385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Lys90Asn
CA256831
NM_000371.3:c.270A>C
CA402157025
NM_000371.3:c.270A>T