Canonical Allele Identifier: PA2573168646
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1518527
ClinVar RCV Id: RCV002021812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Lys29Glu
CA402156485
NM_000371.3:c.85A>G