Canonical Allele Identifier: PA658801678
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 538166
ClinVar RCV Id: RCV000647357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Asp59del
CA658799023
NM_000371.3:c.174_176del