Canonical Allele Identifier: PA297515
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 181690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000362.1:p.Asp119Asn
CA297513
NM_000371.3:c.355G>A